A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562634



Internal ID16003357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88391071..89703421hg38UCSC Ensembl
Innerchr13:89043326..90355675hg19UCSC Ensembl
Innerchr13:87841327..89153676hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg381312351
hg191312350
hg181312350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816745
Samples
Known GenesLINC00353, LINC00433
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562634
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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