A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705748



Internal ID15442400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60605580..60636799hg38UCSC Ensembl
Innerchr18:58272813..58304032hg19UCSC Ensembl
Innerchr18:56423793..56455012hg18UCSC Ensembl
Innerchr18:56423793..56455012hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3831220
hg1931220
hg1831220
hg1731220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520502
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705748
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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