A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561334



Internal ID16002057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23324315..23510670hg38UCSC Ensembl
Innerchr13:23898454..24084809hg19UCSC Ensembl
Innerchr13:22796454..22982809hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38186356
hg19186356
hg18186356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806764
Samples
Known GenesLINC00327, SACS, SACS-AS1, SGCG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561334
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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