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dbVar

Database of genomic structural variation

nsv6460960

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:488

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

Submitted genomic29,348,070-29,348,557

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6460960	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	29,348,070	29,348,557
nsv6460960	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	29,501,003	29,501,490

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17998575	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17998575	Submitted genomic		NC_000012.12:g.293 48070_29348557del	GRCh38 (hg38)		NC_000012.12	Chr12	29,348,070	29,348,557
nssv17998575	Remapped	Perfect	NC_000012.11:g.295 01003_29501490del	GRCh37.p13	First Pass	NC_000012.11	Chr12	29,501,003	29,501,490

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)
nssv17998575	<0.001	12	37952

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