A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1418n54



Internal ID22769313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127176992..127190882hg38UCSC Ensembl
chr10:128975256..128989146hg19UCSC Ensembl
chr10:128865246..128879136hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3813891
hg1913891
hg1813891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552300, nsv552299
Samples
Known GenesDOCK1, FAM196A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1418n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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