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dbVar

Database of genomic structural variation

nsv6710367

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:430

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: 122 SVs from 32 studies. See in: genome view

Submitted genomic111,805,458-111,805,887

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6710367	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	111,805,458	111,805,887
nsv6710367	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	111,524,305	111,524,734

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18472079	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
nssv18472079	Submitted genomic		NC_000003.12:g.111 805458_111805887de l	GRCh38 (hg38)		NC_000003.12	Chr3	111,805,458	111,805,887
nssv18472079	Remapped	Perfect	NC_000003.11:g.111 524305_111524734de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	111,524,305	111,524,734

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)
nssv18472079	0.054	13013	244068

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