A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820869



Internal ID16114825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113971527..114028701hg38UCSC Ensembl
Innerchr13:114740938..114794177hg19UCSC Ensembl
Innerchr13:113759040..113812279hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3857175
hg1953240
hg1853240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563429
Supporting Variants
Samples
Known GenesRASA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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