A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1481n54



Internal ID22769376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133291903..133292176hg38UCSC Ensembl
chr10:135105407..135105680hg19UCSC Ensembl
chr10:134955397..134955670hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38274
hg19274
hg18274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552619, nsv552620
Samples
Known GenesTUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1481n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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