A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562612



Internal ID16350021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85968013..86001734hg38UCSC Ensembl
Innerchr13:86542148..86575869hg19UCSC Ensembl
Innerchr13:85440149..85473870hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3833722
hg1933722
hg1833722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148665
SamplesHGDP00689
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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