A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561435



Internal ID16348844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33325201..33383180hg38UCSC Ensembl
Innerchr13:33899338..33957317hg19UCSC Ensembl
Innerchr13:32797338..32855317hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3857980
hg1957980
hg1857980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807430
Samples
Known GenesSTARD13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561435
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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