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dbVar

Database of genomic structural variation

nsv2760526

Organism: Homo sapiens

Study:nstd130 (Leppa et al. 2016)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:6
Validation:Not tested
Clinical Assertions: No
Region Size:58,466

Publication(s):Leppa et al. 2016

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: 2358 SVs from 95 studies. See in: genome view

Remapped(Score: Perfect):78,267,557-78,326,022

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv2760526	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nsv2760526	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	78,977,274	79,035,739

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv13635830	deletion	SNP array	Probe signal intensity
nssv13635831	deletion	SNP array	Probe signal intensity
nssv13635832	deletion	SNP array	Probe signal intensity
nssv13635833	deletion	SNP array	Probe signal intensity
nssv13635834	deletion	SNP array	Probe signal intensity
nssv13635835	duplication	SNP array	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv13635830	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635831	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635832	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635833	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635834	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635835	Remapped	Perfect	NC_000006.12:g.(?_ 78267557)_(7832602 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,267,557	78,326,022
nssv13635830	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739
nssv13635831	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739
nssv13635832	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739
nssv13635833	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739
nssv13635834	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739
nssv13635835	Submitted genomic		NC_000006.11:g.(?_ 78977274)_(7903573 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	78,977,274	79,035,739

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

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