A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561398



Internal ID16002121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31038259..31072839hg38UCSC Ensembl
Innerchr13:31612396..31646976hg19UCSC Ensembl
Innerchr13:30510396..30544976hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3834581
hg1934581
hg1834581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807247
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561398
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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