A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566056



Internal ID16353465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104680242..104749014hg38UCSC Ensembl
Innerchr14:105146579..105215351hg19UCSC Ensembl
Innerchr14:104217624..104286396hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3868773
hg1968773
hg1868773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3954n54
Supporting Variantsnssv834437
Samples
Known GenesADSSL1, INF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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