nsv6622325

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:28,724

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: 553 SVs from 62 studies. See in: genome view

Remapped(Score: Perfect):70,170,750-70,199,473

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6622325	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nsv6622325	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	70,744,882	70,773,605

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18303292	deletion	OSC5920	SNP array	Probe signal intensity	11
nssv18303627	deletion	OSC5971	SNP array	Probe signal intensity	9
nssv18304418	deletion	OSC6061	SNP array	Probe signal intensity	12
nssv18304713	deletion	OSC6274	SNP array	Probe signal intensity	7
nssv18304827	deletion	OSC6153	SNP array	Probe signal intensity	9
nssv18306515	deletion	OSC6648	SNP array	Probe signal intensity	11
nssv18309013	deletion	OSC7090	SNP array	Probe signal intensity	11
nssv18313354	deletion	OSC7620	SNP array	Probe signal intensity	11
nssv18314881	deletion	OSC8045	SNP array	Probe signal intensity	9
nssv18315341	deletion	OSC8049	SNP array	Probe signal intensity	6
nssv18318572	deletion	OSC8638	SNP array	Probe signal intensity	14
nssv18319613	deletion	OSC8710	SNP array	Probe signal intensity	12
nssv18319645	deletion	OSC8728	SNP array	Probe signal intensity	5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18303292	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18303627	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18304418	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18304713	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18304827	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18306515	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18309013	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18313354	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18314881	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18315341	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18318572	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18319613	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18319645	Remapped	Perfect	NC_000013.11:g.(?_ 70170750)_(7019947 3_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	70,170,750	70,199,473
nssv18303292	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18303627	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18304418	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18304713	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18304827	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18306515	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18309013	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18313354	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18314881	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18315341	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18318572	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18319613	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605
nssv18319645	Submitted genomic		NC_000013.10:g.(?_ 70744882)_(7077360 5_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	70,744,882	70,773,605

dbVar

Database of genomic structural variation

nsv6622325

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