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dbVar

Database of genomic structural variation

nsv6419095

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:574,661

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: 1524 SVs from 88 studies. See in: genome view

Submitted genomic26,431,316-27,005,976

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6419095	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	26,431,316	27,005,976
nsv6419095	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	26,431,314	27,005,974

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18236253	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18236253	Submitted genomic		NC_000009.12:g.264 31316_27005976dup	GRCh38 (hg38)		NC_000009.12	Chr9	26,431,316	27,005,976
nssv18236253	Remapped	Perfect	NC_000009.11:g.264 31314_27005974dup	GRCh37.p13	First Pass	NC_000009.11	Chr9	26,431,314	27,005,974

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)
nssv18236253	<0.001	1	39298

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