A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1080n54



Internal ID22768975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41813135..41861510hg38UCSC Ensembl
chr10:42378699..42427074hg19UCSC Ensembl
chr10:41698705..41747080hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3848376
hg1948376
hg1848376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550606, nsv550607
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1080n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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