A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1353n54



Internal ID22769248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92911092..93050908hg38UCSC Ensembl
chr10:94670849..94810665hg19UCSC Ensembl
chr10:94660829..94800655hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38139817
hg19139817
hg18139827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551942, nsv551941
Samples
Known GenesEXOC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1353n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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