A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1269n54



Internal ID20134693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76496115..76500936hg38UCSC Ensembl
chr10:78255873..78260694hg19UCSC Ensembl
chr10:77925879..77930700hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384822
hg194822
hg184822
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551543, nsv551544
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1269n54
Frequency
Sample Size17421
Observed Gain21
Observed Loss1391
Observed Complex0
Frequencyn/a


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