A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565503



Internal ID16352912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87430015..87732490hg38UCSC Ensembl
Innerchr14:87896359..88198834hg19UCSC Ensembl
Innerchr14:86966112..87268587hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38302476
hg19302476
hg18302476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832161
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565503
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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