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dbVar

Database of genomic structural variation

nsv6449634

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:13,100

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: 159 SVs from 39 studies. See in: genome view

Submitted genomic111,629,001-111,642,100

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6449634	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	111,629,001	111,642,100
nsv6449634	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	114,391,281	114,404,380

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18222315	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18222315	Submitted genomic		NC_000009.12:g.111 629001_111642100du p	GRCh38 (hg38)		NC_000009.12	Chr9	111,629,001	111,642,100
nssv18222315	Remapped	Perfect	NC_000009.11:g.114 391281_114404380du p	GRCh37.p13	First Pass	NC_000009.11	Chr9	114,391,281	114,404,380

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)
nssv18222315	<0.001	2	39222

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