A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1088n54



Internal ID22768983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42155274..42325358hg38UCSC Ensembl
chr10:42650722..42820806hg19UCSC Ensembl
chr10:41970728..42140812hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38170085
hg19170085
hg18170085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550644, nsv550635, nsv550643, nsv550632
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1088n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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