A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561583



Internal ID16348992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46877903..46888665hg38UCSC Ensembl
Innerchr13:47452038..47462800hg19UCSC Ensembl
Innerchr13:46350039..46360801hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3810763
hg1910763
hg1810763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv810013, nssv810014
Samples
Known GenesHTR2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561583
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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