A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561208



Internal ID16001931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19700704..19865880hg38UCSC Ensembl
Innerchr13:20274844..20440020hg19UCSC Ensembl
Innerchr13:19172844..19338020hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38165177
hg19165177
hg18165177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3071n54
Supporting Variantsnssv1175915
Samples1780862415_A
Known GenesPSPC1, ZMYM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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