A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561262



Internal ID16348671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22534697..22925582hg38UCSC Ensembl
Innerchr13:23108836..23499721hg19UCSC Ensembl
Innerchr13:22006836..22397721hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38390886
hg19390886
hg18390886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806198
Samples
Known GenesBASP1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561262
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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