nsv6630183

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:48
Validation:Not tested
Clinical Assertions: No
Region Size:114,264

Publication(s):Zarrei et al. 2023

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: 1457 SVs from 95 studies. See in: genome view

Remapped(Score: Good):9,369,390-9,483,653

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6630183	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nsv6630183	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	9,371,116	9,485,300

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18282290	deletion	OSC2059	SNP array	Probe signal intensity	10
nssv18282430	duplication	OSC2164	SNP array	Probe signal intensity	5
nssv18283192	duplication	OSC2295	SNP array	Probe signal intensity	5
nssv18283735	duplication	OSC2447	SNP array	Probe signal intensity	8
nssv18284603	duplication	OSC2665	SNP array	Probe signal intensity	5
nssv18285472	duplication	OSC2789	SNP array	Probe signal intensity	7
nssv18286352	duplication	OSC2762	SNP array	Probe signal intensity	12
nssv18286653	deletion	OSC2976	SNP array	Probe signal intensity	10
nssv18288443	deletion	OSC3175	SNP array	Probe signal intensity	7
nssv18288507	duplication	OSC3214	SNP array	Probe signal intensity	5
nssv18288557	duplication	OSC0337	SNP array	Probe signal intensity	8
nssv18288606	deletion	OSC3282	SNP array	Probe signal intensity	7
nssv18288654	duplication	OSC3313	SNP array	Probe signal intensity	nssv18289015
nssv18288828	duplication	OSC3216	SNP array	Probe signal intensity	6
nssv18291281	deletion	OSC3658	SNP array	Probe signal intensity	9
nssv18291365	duplication	OSC3715	SNP array	Probe signal intensity	nssv18291362, nssv18291363, nssv18291364
nssv18291946	duplication	OSC3938	SNP array	Probe signal intensity	nssv18291943, nssv18291944, nssv18291945
nssv18292232	duplication	OSC3895	SNP array	Probe signal intensity	10
nssv18292292	duplication	OSC3935	SNP array	Probe signal intensity	14
nssv18292434	deletion	OSC3809	SNP array	Probe signal intensity	8
nssv18293507	duplication	OSC4132	SNP array	Probe signal intensity	nssv18292930, nssv18292931
nssv18293590	duplication	OSC4200	SNP array	Probe signal intensity	11
nssv18295217	deletion	OSC4461	SNP array	Probe signal intensity	nssv18294846, nssv18295218
nssv18295549	duplication	OSC4525	SNP array	Probe signal intensity	nssv18295547, nssv18295548, nssv18295864
nssv18296699	duplication	OSC4869	SNP array	Probe signal intensity	nssv18297267, nssv18297268, nssv18297583
nssv18297188	duplication	OSC0495	SNP array	Probe signal intensity	nssv18296621, nssv18297182, nssv18297514
nssv18297341	duplication	OSC0483	SNP array	Probe signal intensity	nssv18297336
nssv18297758	duplication	OSC4976	SNP array	Probe signal intensity	5
nssv18297983	duplication	OSC4959	SNP array	Probe signal intensity	8
nssv18298243	duplication	OSC5162	SNP array	Probe signal intensity	nssv18298242, nssv18299511
nssv18298293	duplication	OSC0508	SNP array	Probe signal intensity	6
nssv18298296	duplication	OSC4944	SNP array	Probe signal intensity	11
nssv18298418	duplication	OSC5040	SNP array	Probe signal intensity	nssv18297847, nssv18298073
nssv18298775	deletion	OSC5050	SNP array	Probe signal intensity	nssv18298090, nssv18298776
nssv18300616	duplication	OSC5566	SNP array	Probe signal intensity	12
nssv18300722	duplication	OSC5380	SNP array	Probe signal intensity	7
nssv18302882	duplication	OSC0605	SNP array	Probe signal intensity	5
nssv18307227	duplication	OSC0678	SNP array	Probe signal intensity	7
nssv18317524	deletion	OSC0891	SNP array	Probe signal intensity	6
nssv18320095	duplication	OSC1093	SNP array	Probe signal intensity	nssv18320096, nssv18320720, nssv18321383
nssv18320924	deletion	OSC1022	SNP array	Probe signal intensity	nssv18320387, nssv18320923
nssv18321621	deletion	OSC1261	SNP array	Probe signal intensity	6
nssv18322089	duplication	OSC1209	SNP array	Probe signal intensity	10
nssv18323722	duplication	OSC1708	SNP array	Probe signal intensity	9
nssv18323974	duplication	OSC1626	SNP array	Probe signal intensity	nssv18323973, nssv18323975, nssv18324252
nssv18324017	duplication	OSC1659	SNP array	Probe signal intensity	7
nssv18325045	duplication	OSC1973	SNP array	Probe signal intensity	5
nssv18325325	duplication	OSC1926	SNP array	Probe signal intensity	nssv18325324

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18282290	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18282430	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18283192	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18283735	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18284603	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18285472	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18286352	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18286653	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288443	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288507	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288557	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288606	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288654	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18288828	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18291281	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18291365	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18291946	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18292232	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18292292	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18292434	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18293507	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18293590	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18295217	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18295549	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18296699	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18297188	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18297341	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18297758	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18297983	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18298243	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18298293	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18298296	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18298418	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18298775	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18300616	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18300722	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18302882	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18307227	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18317524	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18320095	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18320924	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18321621	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18322089	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18323722	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18323974	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18324017	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18325045	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18325325	Remapped	Good	NC_000004.12:g.(?_ 9369390)_(9483653_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	9,369,390	9,483,653
nssv18282290	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18282430	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18283192	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18283735	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18284603	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18285472	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18286352	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18286653	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288443	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288507	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288557	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288606	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288654	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18288828	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18291281	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18291365	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18291946	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18292232	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18292292	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18292434	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18293507	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18293590	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18295217	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18295549	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18296699	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18297188	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18297341	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18297758	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18297983	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18298243	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18298293	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18298296	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18298418	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18298775	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18300616	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18300722	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18302882	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18307227	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18317524	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18320095	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18320924	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18321621	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18322089	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18323722	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18323974	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18324017	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18325045	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300
nssv18325325	Submitted genomic		NC_000004.11:g.(?_ 9371116)_(9485300_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	9,371,116	9,485,300

dbVar

Database of genomic structural variation

nsv6630183

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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