A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564566



Internal ID16351975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42354354..42442613hg38UCSC Ensembl
Innerchr14:42823557..42911816hg19UCSC Ensembl
Innerchr14:41893307..41981566hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3888260
hg1988260
hg1888260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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