A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562640



Internal ID16350049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89624573..89703421hg38UCSC Ensembl
Innerchr13:90276827..90355675hg19UCSC Ensembl
Innerchr13:89074828..89153676hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3878849
hg1978849
hg1878849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148669
Samples1780862528_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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