A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561338



Internal ID16002061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23901934..24051027hg38UCSC Ensembl
Innerchr13:24476073..24625166hg19UCSC Ensembl
Innerchr13:23374073..23523166hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38149094
hg19149094
hg18149094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806767
Samples
Known GenesANKRD20A19P, SPATA13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561338
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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