A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1015n54



Internal ID22768910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28369346..28376112hg38UCSC Ensembl
chr10:28658275..28665041hg19UCSC Ensembl
chr10:28698281..28705047hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg386767
hg196767
hg186767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550289, nsv550286, nsv550288, nsv550287
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1015n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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