nsv4383109

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:49
Validation:Not tested
Clinical Assertions: No
Region Size:79,545

Publication(s):Zarrei 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: 2466 SVs from 106 studies. See in: genome view

Remapped(Score: Perfect):55,606,555-55,686,099

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4383109	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nsv4383109	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	55,374,031	55,453,575

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611669	copy number loss	1-0653-002	SNP array	Genotyping	28
nssv15612150	copy number loss	1-0013-003	SNP array	Genotyping	27
nssv15612199	copy number loss	1-0660-003	SNP array	Genotyping	23
nssv15612584	copy number loss	1-0699-003	SNP array	Genotyping	19
nssv15612931	copy number loss	1-0692-003	SNP array	Genotyping	17
nssv15612960	copy number loss	1-0694-003	SNP array	Genotyping	23
nssv15613008	copy number loss	1-0696-003	SNP array	Genotyping	21
nssv15613130	copy number loss	1-0677-001	SNP array	Genotyping	26
nssv15613358	copy number loss	1-0701-003	SNP array	Genotyping	20
nssv15613409	copy number loss	1-0703-003	SNP array	Genotyping	27
nssv15613566	copy number loss	1-0690-003	SNP array	Genotyping	14
nssv15624318	copy number loss	1-0045-002	SNP array	Genotyping	24
nssv15624547	copy number loss	1-0045-004	SNP array	Genotyping	27
nssv15624593	copy number loss	1-0301-003	SNP array	Genotyping	32
nssv15629844	copy number loss	1-0083-004	SNP array	Genotyping	23
nssv15631457	copy number loss	1-0627-007	SNP array	Genotyping	22
nssv15632235	copy number loss	10-1090-004	SNP array	Genotyping	26
nssv15632296	copy number loss	10-1104-002	SNP array	Genotyping	24
nssv15633020	copy number loss	10-1090-005	SNP array	Genotyping	18
nssv15647345	copy number loss	2-1238-003	SNP array	Genotyping	19
nssv15652258	copy number loss	2-1550-003	SNP array	Genotyping	21
nssv15653035	copy number loss	2-1584-003	SNP array	Genotyping	20
nssv15654774	copy number loss	3-0269-001	SNP array	Genotyping	17
nssv15656345	copy number loss	4-0027-001	SNP array	Genotyping	22
nssv15657221	copy number loss	3-0306-001	SNP array	Genotyping	21
nssv15657340	copy number loss	3-0380-002	SNP array	Genotyping	28
nssv15657474	copy number loss	4-0027-002	SNP array	Genotyping	22
nssv15658521	copy number loss	4-0046-004	SNP array	Genotyping	25
nssv15661536	copy number loss	4-0027-004	SNP array	Genotyping	23
nssv15661849	copy number loss	4-0042-001	SNP array	Genotyping	16
nssv15661863	copy number loss	4-0042-003	SNP array	Genotyping	15
nssv15661879	copy number loss	4-0042-004	SNP array	Genotyping	16
nssv15663041	copy number loss	4-0046-001	SNP array	Genotyping	29
nssv15663961	copy number loss	5-0143-003	SNP array	Genotyping	22
nssv15664398	copy number loss	7-0065-003	SNP array	Genotyping	20
nssv15664473	copy number loss	7-0075-003	SNP array	Genotyping	17
nssv15665214	copy number loss	7-0069-003	SNP array	Genotyping	21
nssv15694085	copy number loss	215689	SNP array	Genotyping	18
nssv15694675	copy number loss	211008	SNP array	Genotyping	23
nssv15695619	copy number loss	217438	SNP array	Genotyping	25
nssv15695822	copy number loss	207951	SNP array	Genotyping	22
nssv15695835	copy number loss	212972	SNP array	Genotyping	20
nssv15696750	copy number loss	217440	SNP array	Genotyping	23
nssv15698029	copy number loss	200039	SNP array	Genotyping	25
nssv15698309	copy number loss	139979	SNP array	Genotyping	26
nssv15698416	copy number loss	177296	SNP array	Genotyping	18
nssv15699674	copy number loss	213684	SNP array	Genotyping	22
nssv15699844	copy number loss	211845	SNP array	Genotyping	18
nssv15701851	copy number loss	214095	SNP array	Genotyping	23

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611669	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15612150	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15612199	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15612584	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15612931	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15612960	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15613008	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15613130	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15613358	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15613409	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15613566	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15624318	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15624547	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15624593	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15629844	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15631457	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15632235	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15632296	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15633020	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15647345	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15652258	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15653035	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15654774	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15656345	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15657221	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15657340	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15657474	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15658521	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15661536	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15661849	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15661863	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15661879	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15663041	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15663961	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15664398	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15664473	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15665214	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15694085	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15694675	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15695619	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15695822	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15695835	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15696750	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15698029	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15698309	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15698416	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15699674	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15699844	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15701851	Remapped	Perfect	NC_000011.10:g.(?_ 55606555)_(5568609 9_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	55,606,555	55,686,099
nssv15611669	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15612150	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15612199	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15612584	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15612931	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15612960	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15613008	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15613130	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15613358	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15613409	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15613566	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15624318	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15624547	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15624593	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15629844	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15631457	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15632235	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15632296	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15633020	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15647345	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15652258	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15653035	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15654774	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15656345	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15657221	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15657340	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15657474	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15658521	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15661536	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15661849	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15661863	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15661879	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15663041	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15663961	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15664398	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15664473	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15665214	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15694085	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15694675	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15695619	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15695822	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15695835	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15696750	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15698029	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15698309	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15698416	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15699674	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15699844	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575
nssv15701851	Submitted genomic		NC_000011.9:g.(?_5 5374031)_(55453575 _?)del	GRCh37 (hg19)		NC_000011.9	Chr11	55,374,031	55,453,575

dbVar

Database of genomic structural variation

nsv4383109

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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