A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703447



Internal ID15440099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86031153..86090870hg38UCSC Ensembl
Innerchr13:86605288..86665005hg19UCSC Ensembl
Innerchr13:85503289..85563006hg18UCSC Ensembl
Innerchr13:85503289..85563006hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3859718
hg1959718
hg1859718
hg1759718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527068
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703447
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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