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dbVar

Database of genomic structural variation

nsv6914392

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:110

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: 107 SVs from 21 studies. See in: genome view

Submitted genomic87,818,064-87,818,173

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6914392	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	87,818,064	87,818,173
nsv6914392	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	87,528,956	87,529,065

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18583746	duplication	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
nssv18583746	Submitted genomic		NC_000011.10:g.878 18064_87818173dup	GRCh38 (hg38)		NC_000011.10	Chr11	87,818,064	87,818,173
nssv18583746	Remapped	Perfect	NC_000011.9:g.8752 8956_87529065dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	87,528,956	87,529,065

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)
nssv18583746	4e-06	1	223140

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