A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561462



Internal ID16348871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34253465..34291583hg38UCSC Ensembl
Innerchr13:34827602..34865720hg19UCSC Ensembl
Innerchr13:33725602..33763720hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3838119
hg1938119
hg1838119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807648
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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