A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562384



Internal ID16349793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697665..77698337hg38UCSC Ensembl
Innerchr13:78271800..78272472hg19UCSC Ensembl
Innerchr13:77169801..77170473hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38673
hg19673
hg18673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3263n54
Supporting Variantsnssv815810
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562384
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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