A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527344



Internal ID15454637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17091398..17114565hg38UCSC Ensembl
Innerchr20:17072043..17095210hg19UCSC Ensembl
Innerchr20:17020043..17043210hg18UCSC Ensembl
Innerchr20:17020043..17043210hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3823168
hg1923168
hg1823168
hg1723168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703770
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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