A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938633



Internal ID16232589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924061..19924592hg38UCSC Ensembl
Innerchr20:19904705..19905236hg19UCSC Ensembl
Innerchr20:19852705..19853236hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38532
hg19532
hg18532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585682
Supporting Variants
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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