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dbVar

Database of genomic structural variation

nsv3063836

Organism: Homo sapiens

Study:nstd140 (Fan et al. 2017)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:8,501

Publication(s):Fan et al. 2017

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: 709 SVs from 67 studies. See in: genome view

Submitted genomic8,084,567-8,093,067

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3063836	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	8,084,567	8,093,067
nsv3063836	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	7,942,089	7,950,589

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14034690	deletion	NA12878	Sequencing	Local sequence assembly	15,093

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14034690	Submitted genomic		NC_000008.11:g.808 4567_8093067del	GRCh38 (hg38)		NC_000008.11	Chr8	8,084,567	8,093,067
nssv14034690	Remapped	Perfect	NC_000008.10:g.794 2089_7950589del	GRCh37.p13	First Pass	NC_000008.10	Chr8	7,942,089	7,950,589

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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