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dbVar

Database of genomic structural variation

nsv6112823

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:20,389

Description:nsv5432807 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 207 SVs from 48 studies. See in: genome view

Remapped(Score: Perfect):74,068,712-74,089,100

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112823	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	74,068,712	74,089,100
nsv6112823	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	74,361,053	74,381,441

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17968508	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17968508	Remapped	Perfect	GRCh38.p12	First Pass	NC_000015.10	Chr15	74,068,712	74,089,100
nssv17968508	Submitted genomic		GRCh37 (hg19)		NC_000015.9	Chr15	74,361,053	74,381,441

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17968508	0.495	3029	6118

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