A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566159



Internal ID16006882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105149311..105219528hg38UCSC Ensembl
Innerchr14:105615648..105685865hg19UCSC Ensembl
Innerchr14:104686693..104756910hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3870218
hg1970218
hg1870218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3977n54
Supporting Variantsnssv1148634, nssv1148635
SamplesHGDP00679, HGDP00417
Known GenesBRF1, JAG2, MIR6765, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566159
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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