Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4175145

Organism: Homo sapiens

Study:nstd166 (gnomAD Structural Variants)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,479

Publication(s):gnomAD_Structural_Variants

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: 32 SVs from 10 studies. See in: genome view

Remapped(Score: Perfect):23,441,451-23,445,929

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4175145	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	23,441,451	23,445,929
nsv4175145	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000010.10	Chr10	23,730,380	23,734,858

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15945877	duplication	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15945877	Remapped	Perfect	NC_000010.11:g.234 41451_23445929dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	23,441,451	23,445,929
nssv15945877	Submitted genomic		NC_000010.10:g.237 30380_23734858dup	GRCh37.p13		NC_000010.10	Chr10	23,730,380	23,734,858

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv15945877	0.005	109	21694

You are here: NCBI