A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937456



Internal ID15884726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5546530..5574162hg38UCSC Ensembl
Innerchr20:5527176..5554808hg19UCSC Ensembl
Innerchr20:5475176..5502808hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3827633
hg1927633
hg1827633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585328
Supporting Variants
Samples
Known GenesGPCPD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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