A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585256



Internal ID16372665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1914283..1914987hg38UCSC Ensembl
Innerchr20:1894929..1895633hg19UCSC Ensembl
Innerchr20:1842929..1843633hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38705
hg19705
hg18705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7437n54
Supporting Variantsnssv937234, nssv937229, nssv937233, nssv937235, nssv937236, nssv937230, nssv937231, nssv937232
Samples
Known GenesSIRPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585256
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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