A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683313



Internal ID15419965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13065384..13084531hg38UCSC Ensembl
Innerchr7:13105009..13124156hg19UCSC Ensembl
Innerchr7:13071534..13090681hg18UCSC Ensembl
Innerchr7:12878249..12897396hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3819148
hg1919148
hg1819148
hg1719148
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516983
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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