A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527764



Internal ID15455057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51713165..51715804hg38UCSC Ensembl
Innerchr20:50329704..50332343hg19UCSC Ensembl
Innerchr20:49763111..49765750hg18UCSC Ensembl
Innerchr20:49763111..49765750hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382640
hg192640
hg182640
hg172640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704252
Samples
Known GenesATP9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527764
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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