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dbVar

Database of genomic structural variation

nsv6711989

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:176,893

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: 1734 SVs from 91 studies. See in: genome view

Submitted genomic241,731,561-241,908,453

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6711989	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	241,731,561	241,908,453
nsv6711989	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	242,670,976	242,850,604

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18665757	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
nssv18665757	Submitted genomic		NC_000002.12:g.241 731561_241908453du p	GRCh38 (hg38)		NC_000002.12	Chr2	241,731,561	241,908,453
nssv18665757	Remapped	Good	NC_000002.11:g.242 670976_242850604du p	GRCh37.p13	First Pass	NC_000002.11	Chr2	242,670,976	242,850,604

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)
nssv18665757	4e-06	1	275548

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