A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561190



Internal ID16348599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18967770..19052788hg38UCSC Ensembl
Innerchr13:19541910..19626928hg19UCSC Ensembl
Innerchr13:18439910..18524928hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3885019
hg1985019
hg1885019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3069n54
Supporting Variantsnssv1175911
SamplesHGDP00056
Known GenesLINC00442
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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