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dbVar

Database of genomic structural variation

nsv6389239

Organism: Homo sapiens

Study:nstd223 (Sedlazeck et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:103,900

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: 491 SVs from 64 studies. See in: genome view

Submitted genomic67,374,701-67,478,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6389239	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	67,374,701	67,478,600
nsv6389239	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	68,240,419	68,344,318

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18211630	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18211630	Submitted genomic		NC_000004.12:g.673 74701_67478600dup	GRCh38 (hg38)		NC_000004.12	Chr4	67,374,701	67,478,600
nssv18211630	Remapped	Perfect	NC_000004.11:g.682 40419_68344318dup	GRCh37.p13	First Pass	NC_000004.11	Chr4	68,240,419	68,344,318

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)
nssv18211630	<0.001	2	39254

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