A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565189



Internal ID16352598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75053362..75057829hg38UCSC Ensembl
Innerchr14:75520065..75524532hg19UCSC Ensembl
Innerchr14:74589818..74594285hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384468
hg194468
hg184468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3778n54
Supporting Variantsnssv829523
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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