A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683640



Internal ID15420292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:72985844..73024727hg38UCSC Ensembl
Innerchr13:73559982..73598865hg19UCSC Ensembl
Innerchr13:72457983..72496866hg18UCSC Ensembl
Innerchr13:72457983..72496866hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3838884
hg1938884
hg1838884
hg1738884
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517408
Supporting Variants
Samples
Known GenesPIBF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683640
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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