A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517785



Internal ID15098392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35556975..35564866hg38UCSC Ensembl
Innerchr20:34144746..34152782hg19UCSC Ensembl
Innerchr20:33608160..33616196hg18UCSC Ensembl
Innerchr20:33608160..33616196hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387892
hg198037
hg188037
hg178037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653243, nssv694016, nssv666260, nssv680799, nssv663525, nssv654499
Samples
Known GenesERGIC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517785
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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