A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3977n54



Internal ID18996153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105149311..105219528hg38UCSC Ensembl
chr14:105615648..105685865hg19UCSC Ensembl
chr14:104686693..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 Variants
Supporting Variantsnsv566160, nsv566159
SamplesHGDP00417, HGDP00679
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)dgv3977n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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