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dbVar

Database of genomic structural variation

nsv6546000

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:4,500

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: 109 SVs from 23 studies. See in: genome view

Submitted genomic46,539,801-46,544,300

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6546000	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	46,539,801	46,544,300
nsv6546000	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	45,168,440	45,172,939

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18202912	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18202912	Submitted genomic		NC_000020.11:g.465 39801_46544300dup	GRCh38 (hg38)		NC_000020.11	Chr20	46,539,801	46,544,300
nssv18202912	Remapped	Perfect	NC_000020.10:g.451 68440_45172939dup	GRCh37.p13	First Pass	NC_000020.10	Chr20	45,168,440	45,172,939

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)
nssv18202912	<0.001	4	39220

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