nsv3318316

Organism: Homo sapiens

Study:nstd157 (Frenkel et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:72
Validation:Not tested
Clinical Assertions: No
Region Size:45,818

Publication(s):Frenkel et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 633 SVs from 74 studies. See in: genome view

Remapped(Score: Perfect):41,146,665-41,192,482

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3318316	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nsv3318316	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	41,615,868	41,661,685

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14467637	copy number loss	M1153	SNP array	SNP genotyping analysis	12
nssv14467693	copy number loss	M1336	SNP array	SNP genotyping analysis	19
nssv14467743	copy number loss	M2102	SNP array	SNP genotyping analysis	11
nssv14467806	copy number loss	M2109	SNP array	SNP genotyping analysis	11
nssv14467840	copy number loss	M2112	SNP array	SNP genotyping analysis	22
nssv14467906	copy number loss	M2116	SNP array	SNP genotyping analysis	21
nssv14468127	copy number loss	M2130	SNP array	SNP genotyping analysis	26
nssv14468177	copy number loss	M2133	SNP array	SNP genotyping analysis	15
nssv14468191	copy number loss	M2134	SNP array	SNP genotyping analysis	25
nssv14468216	copy number loss	M2135	SNP array	SNP genotyping analysis	17
nssv14468286	copy number loss	M2137	SNP array	SNP genotyping analysis	11
nssv14468507	copy number loss	M2160	SNP array	SNP genotyping analysis	22
nssv14468673	copy number loss	M2175	SNP array	SNP genotyping analysis	20
nssv14468728	copy number loss	M2177	SNP array	SNP genotyping analysis	15
nssv14468867	copy number loss	M2187	SNP array	SNP genotyping analysis	20
nssv14468888	copy number loss	M2188	SNP array	SNP genotyping analysis	27
nssv14468928	copy number loss	M2191	SNP array	SNP genotyping analysis	24
nssv14468968	copy number loss	M2193	SNP array	SNP genotyping analysis	17
nssv14469026	copy number loss	M2196	SNP array	SNP genotyping analysis	17
nssv14469087	copy number loss	M2199	SNP array	SNP genotyping analysis	15
nssv14469170	copy number loss	M2212	SNP array	SNP genotyping analysis	15
nssv14469240	copy number loss	M2218	SNP array	SNP genotyping analysis	21
nssv14469288	copy number loss	M2221	SNP array	SNP genotyping analysis	11
nssv14469308	copy number loss	M2224	SNP array	SNP genotyping analysis	16
nssv14469410	copy number loss	M2234	SNP array	SNP genotyping analysis	10
nssv14469438	copy number loss	M2237	SNP array	SNP genotyping analysis	10
nssv14469482	copy number loss	M2240	SNP array	SNP genotyping analysis	13
nssv14469501	copy number loss	M2243	SNP array	SNP genotyping analysis	24
nssv14469520	copy number loss	M2245	SNP array	SNP genotyping analysis	10
nssv14469532	copy number loss	M2247	SNP array	SNP genotyping analysis	20
nssv14469595	copy number loss	M2251	SNP array	SNP genotyping analysis	12
nssv14469646	copy number loss	M2257	SNP array	SNP genotyping analysis	24
nssv14469713	copy number loss	M2260	SNP array	SNP genotyping analysis	17
nssv14469754	copy number loss	M2266	SNP array	SNP genotyping analysis	28
nssv14469878	copy number loss	M2281	SNP array	SNP genotyping analysis	30
nssv14469940	copy number loss	M2291	SNP array	SNP genotyping analysis	38
nssv14470027	copy number loss	M2299	SNP array	SNP genotyping analysis	17
nssv14470060	copy number loss	M2304	SNP array	SNP genotyping analysis	18
nssv14470145	copy number loss	M2315	SNP array	SNP genotyping analysis	17
nssv14470212	copy number loss	M2321	SNP array	SNP genotyping analysis	20
nssv14470235	copy number loss	M2322	SNP array	SNP genotyping analysis	16
nssv14470269	copy number loss	M2324	SNP array	SNP genotyping analysis	19
nssv14470289	copy number loss	M2326	SNP array	SNP genotyping analysis	18
nssv14470321	copy number loss	M2331	SNP array	SNP genotyping analysis	21
nssv14470345	copy number loss	M2333	SNP array	SNP genotyping analysis	19
nssv14470467	copy number loss	M2342	SNP array	SNP genotyping analysis	13
nssv14470511	copy number loss	M2354	SNP array	SNP genotyping analysis	21
nssv14470679	copy number loss	M2369	SNP array	SNP genotyping analysis	22
nssv14470779	copy number loss	M2377	SNP array	SNP genotyping analysis	14
nssv14470793	copy number loss	M2378	SNP array	SNP genotyping analysis	16
nssv14470808	copy number loss	M2383	SNP array	SNP genotyping analysis	23
nssv14470867	copy number loss	M2388	SNP array	SNP genotyping analysis	18
nssv14470884	copy number loss	M2390	SNP array	SNP genotyping analysis	13
nssv14470934	copy number loss	M2394	SNP array	SNP genotyping analysis	15
nssv14470968	copy number loss	M2396	SNP array	SNP genotyping analysis	16
nssv14470984	copy number loss	M2397	SNP array	SNP genotyping analysis	13
nssv14471010	copy number loss	M2399	SNP array	SNP genotyping analysis	15
nssv14471090	copy number loss	M2406	SNP array	SNP genotyping analysis	18
nssv14471168	copy number loss	M2420	SNP array	SNP genotyping analysis	24
nssv14471189	copy number loss	M2421	SNP array	SNP genotyping analysis	18
nssv14471227	copy number loss	M2423	SNP array	SNP genotyping analysis	15
nssv14471285	copy number loss	M2430	SNP array	SNP genotyping analysis	16
nssv14471413	copy number loss	M2443	SNP array	SNP genotyping analysis	15
nssv14471461	copy number loss	M2454	SNP array	SNP genotyping analysis	17
nssv14471601	copy number loss	M2465	SNP array	SNP genotyping analysis	20
nssv14471619	copy number loss	M2466	SNP array	SNP genotyping analysis	14
nssv14471635	copy number loss	M2468	SNP array	SNP genotyping analysis	15
nssv14471649	copy number loss	M2471	SNP array	SNP genotyping analysis	19
nssv14471665	copy number loss	M2472	SNP array	SNP genotyping analysis	12
nssv14471702	copy number loss	M2482	SNP array	SNP genotyping analysis	21
nssv14471805	copy number loss	M2495	SNP array	SNP genotyping analysis	13
nssv14471984	copy number loss	M2513	SNP array	SNP genotyping analysis	19

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv14467637	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467693	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467743	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467806	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467840	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467906	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468127	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468177	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468191	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468216	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468286	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468507	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468673	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468728	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468867	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468888	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468928	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14468968	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469026	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469087	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469170	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469240	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469288	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469308	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469410	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469438	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469482	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469501	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469520	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469532	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469595	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469646	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469713	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469754	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469878	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14469940	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470027	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470060	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470145	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470212	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470235	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470269	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470289	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470321	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470345	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470467	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470511	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470679	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470779	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470793	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470808	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470867	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470884	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470934	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470968	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14470984	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471010	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471090	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471168	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471189	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471227	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471285	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471413	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471461	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471601	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471619	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471635	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471649	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471665	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471702	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471805	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14471984	Remapped	Perfect	NC_000014.9:g.(?_4 1146665)_(41192482 _?)del	GRCh38.p12	First Pass	NC_000014.9	Chr14	41,146,665	41,192,482
nssv14467637	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14467693	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14467743	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14467806	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14467840	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14467906	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468127	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468177	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468191	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468216	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468286	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468507	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468673	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468728	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468867	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468888	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468928	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14468968	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469026	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469087	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469170	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469240	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469288	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469308	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469410	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469438	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469482	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685
nssv14469501	Submitted genomic		NC_000014.8:g.(?_4 1615868)_(41661685 _?)del	GRCh37 (hg19)		NC_000014.8	Chr14	41,615,868	41,661,685

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dbVar

Database of genomic structural variation

nsv3318316

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant