A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820868



Internal ID15768138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113970798..114076351hg38UCSC Ensembl
Innerchr13:114740209..114841826hg19UCSC Ensembl
Innerchr13:113758311..113859928hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38105554
hg19101618
hg18101618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563428
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)nssv820868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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