A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819921



Internal ID16113877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110943052..110972744hg38UCSC Ensembl
Innerchr13:111595399..111625091hg19UCSC Ensembl
Innerchr13:110393400..110423092hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3829693
hg1929693
hg1829693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563164
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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