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dbVar

Database of genomic structural variation

nsv6645491

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:64

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: 154 SVs from 22 studies. See in: genome view

Submitted genomic179,337,463-179,337,526

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6645491	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	179,337,463	179,337,526
nsv6645491	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	179,306,598	179,306,661

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18364677	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18364677	Submitted genomic		NC_000001.11:g.179 337463_179337526de l	GRCh38 (hg38)		NC_000001.11	Chr1	179,337,463	179,337,526
nssv18364677	Remapped	Perfect	NC_000001.10:g.179 306598_179306661de l	GRCh37.p13	First Pass	NC_000001.10	Chr1	179,306,598	179,306,661

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)
nssv18364677	0.005	1178	240734

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