A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701238



Internal ID15437890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70843789..70856453hg38UCSC Ensembl
Innerchr13:71417921..71430585hg19UCSC Ensembl
Innerchr13:70315922..70328586hg18UCSC Ensembl
Innerchr13:70315922..70328586hg17UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812665
hg1912665
hg1812665
hg1712665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525164
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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