A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565997



Internal ID16353406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521722..103521999hg38UCSC Ensembl
Innerchr14:103988059..103988336hg19UCSC Ensembl
Innerchr14:103057812..103058089hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38278
hg19278
hg18278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834353
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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