A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1373n54



Internal ID22769268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100436314..100446332hg38UCSC Ensembl
chr10:102196071..102206089hg19UCSC Ensembl
chr10:102186061..102196079hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3810019
hg1910019
hg1810019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552049, nsv552050
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1373n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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