A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561514



Internal ID16348923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38459105..38490149hg38UCSC Ensembl
Innerchr13:39033242..39064286hg19UCSC Ensembl
Innerchr13:37931242..37962286hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3831045
hg1931045
hg1831045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3124n54
Supporting Variantsnssv808004
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561514
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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