A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657263



Internal ID15393915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111588392..111602105hg38UCSC Ensembl
Innerchr7:111228448..111242161hg19UCSC Ensembl
Innerchr7:111015684..111029397hg18UCSC Ensembl
Innerchr7:110822399..110836112hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813714
hg1913714
hg1813714
hg1713714
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657263
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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