A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562620



Internal ID16350029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86488396..86659712hg38UCSC Ensembl
Innerchr13:87140651..87311967hg19UCSC Ensembl
Innerchr13:85938652..86109968hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38171317
hg19171317
hg18171317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816731
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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