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dbVar

Database of genomic structural variation

nsv6455602

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:2,200

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

Submitted genomic76,044,401-76,046,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6455602	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	76,044,401	76,046,600
nsv6455602	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	76,438,181	76,440,380

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18004066	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18004066	Submitted genomic		NC_000012.12:g.760 44401_76046600del	GRCh38 (hg38)		NC_000012.12	Chr12	76,044,401	76,046,600
nssv18004066	Remapped	Perfect	NC_000012.11:g.764 38181_76440380del	GRCh37.p13	First Pass	NC_000012.11	Chr12	76,438,181	76,440,380

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)
nssv18004066	<0.001	3	38940

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