A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585329



Internal ID16372738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5566048..5630091hg38UCSC Ensembl
Innerchr20:5546694..5610737hg19UCSC Ensembl
Innerchr20:5494694..5558737hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3864044
hg1964044
hg1864044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937457
Samples
Known GenesGPCPD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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