nsv6631444

Organism: Homo sapiens

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

Variant Calls:13
Validation:Not tested
Clinical Assertions: No
Region Size:42,356

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: 1176 SVs from 92 studies. See in: genome view

Remapped(Score: Perfect):66,292,183-66,334,538

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6631444	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nsv6631444	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	67,002,076	67,044,431

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18281689	deletion	OSC2088	SNP array	Probe signal intensity	6
nssv18282111	deletion	OSC2165	SNP array	Probe signal intensity	5
nssv18282811	deletion	OSC2225	SNP array	Probe signal intensity	nssv18282189, nssv18282810
nssv18285505	deletion	OSC2813	SNP array	Probe signal intensity	8
nssv18287474	deletion	OSC2911	SNP array	Probe signal intensity	9
nssv18288597	deletion	OSC3275	SNP array	Probe signal intensity	8
nssv18294091	deletion	OSC4304	SNP array	Probe signal intensity	10
nssv18296101	deletion	OSC4453	SNP array	Probe signal intensity	nssv18294839, nssv18294521, nssv18294522
nssv18302072	deletion	OSC5681	SNP array	Probe signal intensity	6
nssv18313872	deletion	OSC0830	SNP array	Probe signal intensity	6
nssv18315219	deletion	OSC0831	SNP array	Probe signal intensity	8
nssv18317292	deletion	OSC0877	SNP array	Probe signal intensity	9
nssv18321325	deletion	OSC1305	SNP array	Probe signal intensity	10

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18281689	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18282111	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18282811	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18285505	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18287474	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18288597	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18294091	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18296101	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18302072	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18313872	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18315219	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18317292	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18321325	Remapped	Perfect	NC_000006.12:g.(?_ 66292183)_(6633453 8_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	66,292,183	66,334,538
nssv18281689	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18282111	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18282811	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18285505	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18287474	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18288597	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18294091	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18296101	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18302072	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18313872	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18315219	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18317292	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431
nssv18321325	Submitted genomic		NC_000006.11:g.(?_ 67002076)_(6704443 1_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	67,002,076	67,044,431

dbVar

Database of genomic structural variation

nsv6631444

Links to Other Resources

Genome View

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