A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565367



Internal ID16352776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83166272..83314261hg38UCSC Ensembl
Innerchr14:83632616..83780605hg19UCSC Ensembl
Innerchr14:82702369..82850358hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38147990
hg19147990
hg18147990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831382
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565367
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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