A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562207



Internal ID16002930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69623503..69714126hg38UCSC Ensembl
Innerchr13:70197635..70288258hg19UCSC Ensembl
Innerchr13:69095636..69186259hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3890624
hg1990624
hg1890624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813691
Samples
Known GenesKLHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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