A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656332



Internal ID15392984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59986626..59995947hg38UCSC Ensembl
Innerchr18:57653858..57663179hg19UCSC Ensembl
Innerchr18:55804838..55814159hg18UCSC Ensembl
Innerchr18:55804838..55814159hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg389322
hg199322
hg189322
hg179322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515764
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656332
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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