A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565883



Internal ID16353292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101700166..101713577hg38UCSC Ensembl
Innerchr14:102166503..102179914hg19UCSC Ensembl
Innerchr14:101236256..101249667hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3813412
hg1913412
hg1813412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833727
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565883
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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