A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561393



Internal ID16348802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30152756..30173985hg38UCSC Ensembl
Innerchr13:30726893..30748122hg19UCSC Ensembl
Innerchr13:29624893..29646122hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3821230
hg1921230
hg1821230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807244
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561393
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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