A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562201



Internal ID16349610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68942082..68985238hg38UCSC Ensembl
Innerchr13:69516214..69559370hg19UCSC Ensembl
Innerchr13:68414215..68457371hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3843157
hg1943157
hg1843157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813688
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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