A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561390



Internal ID16348799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28912107..28988943hg38UCSC Ensembl
Innerchr13:29486244..29563080hg19UCSC Ensembl
Innerchr13:28384244..28461080hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3876837
hg1976837
hg1876837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807241, nssv807242
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561390
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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