A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701660



Internal ID15438312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95348495..95394816hg38UCSC Ensembl
Innerchr13:96000749..96047070hg19UCSC Ensembl
Innerchr13:94798750..94845071hg18UCSC Ensembl
Innerchr13:94798750..94845071hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3846322
hg1946322
hg1846322
hg1746322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525525
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701660
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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