A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562271



Internal ID16349680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71551509..71657714hg38UCSC Ensembl
Innerchr13:72125641..72231846hg19UCSC Ensembl
Innerchr13:71023642..71129847hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38106206
hg19106206
hg18106206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3243n54
Supporting Variantsnssv813827
Samples
Known GenesDACH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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