A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564121



Internal ID16351530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27174241..27471026hg38UCSC Ensembl
Innerchr14:27643447..27940232hg19UCSC Ensembl
Innerchr14:26713287..27010072hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38296786
hg19296786
hg18296786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825064
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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