A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806175



Internal ID16100131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21153703..21158036hg38UCSC Ensembl
Innerchr13:21727842..21732175hg19UCSC Ensembl
Innerchr13:20625842..20630175hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg384334
hg194334
hg184334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561251
Supporting Variants
Samples
Known GenesSKA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806175
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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