A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564557



Internal ID16351966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41209263..41265545hg38UCSC Ensembl
Innerchr14:41678466..41734748hg19UCSC Ensembl
Innerchr14:40748216..40804498hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3856283
hg1956283
hg1856283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3670n54
Supporting Variantsnssv827220
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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