A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562518



Internal ID16349927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83523737..83583792hg38UCSC Ensembl
Innerchr13:84097872..84157927hg19UCSC Ensembl
Innerchr13:82995873..83055928hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3860056
hg1960056
hg1860056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3287n54
Supporting Variantsnssv1148521
SamplesHGDP01057
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562518
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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