A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565009



Internal ID16352418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70214320..70222673hg38UCSC Ensembl
Innerchr14:70681037..70689390hg19UCSC Ensembl
Innerchr14:69750790..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg388354
hg198354
hg188354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3745n54
Supporting Variantsnssv828826
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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