A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1401n54



Internal ID22769296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115722372..115776738hg38UCSC Ensembl
chr10:117481882..117536249hg19UCSC Ensembl
chr10:117471872..117526239hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3854367
hg1954368
hg1854368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552210, nsv552209, nsv552208
SamplesHGDP01185
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1401n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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