A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566065



Internal ID16006788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104697195..104710846hg38UCSC Ensembl
Innerchr14:105163532..105177183hg19UCSC Ensembl
Innerchr14:104234577..104248228hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3813652
hg1913652
hg1813652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3955n54
Supporting Variantsnssv834446
Samples
Known GenesINF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566065
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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