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dbVar

Database of genomic structural variation

nsv6606752

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:3,701

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: 88 SVs from 20 studies. See in: genome view

Submitted genomic155,267,584-155,271,284

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6606752	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	155,267,584	155,271,284
nsv6606752	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	155,588,718	155,592,418

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18139773	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18139773	Submitted genomic		NC_000006.12:g.155 267584_155271284de l	GRCh38 (hg38)		NC_000006.12	Chr6	155,267,584	155,271,284
nssv18139773	Remapped	Perfect	NC_000006.11:g.155 588718_155592418de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	155,588,718	155,592,418

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)
nssv18139773	<0.001	1	39176

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