A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561288



Internal ID16348697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22954546..23290518hg38UCSC Ensembl
Innerchr13:23528685..23864657hg19UCSC Ensembl
Innerchr13:22426685..22762657hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38335973
hg19335973
hg18335973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175923
SamplesNINDS_163
Known GenesSGCG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561288
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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