A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1065n54



Internal ID22768960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38779418..38861089hg38UCSC Ensembl
chr10:39072549..39154220hg19UCSC Ensembl
chr10:39112555..39194226hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3881672
hg1981672
hg1881672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550546, nsv550545, nsv550543, nsv550544
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1065n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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