A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567134



Internal ID16354543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106873771..106880863hg38UCSC Ensembl
Innerchr14:107281980..107289053hg19UCSC Ensembl
Innerchr14:106353025..106360098hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg387093
hg197074
hg187074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv836865
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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