A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527759



Internal ID15455052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63012978..63019990hg38UCSC Ensembl
Innerchr20:61644330..61651342hg19UCSC Ensembl
Innerchr20:61114775..61121787hg18UCSC Ensembl
Innerchr20:61114775..61121787hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387013
hg197013
hg187013
hg177013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704246
Samples
Known GenesLOC63930
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527759
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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