A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938617



Internal ID16232573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924061..19924322hg38UCSC Ensembl
Innerchr20:19904705..19904966hg19UCSC Ensembl
Innerchr20:19852705..19852966hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38262
hg19262
hg18262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585680
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)nssv938617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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