A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1016n54



Internal ID22768911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28371674..28376112hg38UCSC Ensembl
chr10:28660603..28665041hg19UCSC Ensembl
chr10:28700609..28705047hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384439
hg194439
hg184439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550291, nsv550292, nsv550290
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1016n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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