A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585330



Internal ID16372739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5601811..5688068hg38UCSC Ensembl
Innerchr20:5582457..5668714hg19UCSC Ensembl
Innerchr20:5530457..5616714hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3886258
hg1986258
hg1886258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937458
Samples
Known GenesGPCPD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585330
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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