A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944137



Internal ID16238093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64036665..64048475hg38UCSC Ensembl
Innerchr20:62668018..62679828hg19UCSC Ensembl
Innerchr20:62138462..62150272hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811811
hg1911811
hg1811811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586717
Supporting Variants
Samples
Known GenesLINC00176, SOX18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv944137
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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