A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562097



Internal ID16349506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66217001..66269164hg38UCSC Ensembl
Innerchr13:66791133..66843296hg19UCSC Ensembl
Innerchr13:65689134..65741297hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3852164
hg1952164
hg1852164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813156
Samples
Known GenesMIR4704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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