A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1140n54



Internal ID22769035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52764898..52772139hg38UCSC Ensembl
chr10:54524658..54531899hg19UCSC Ensembl
chr10:54194664..54201905hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg387242
hg197242
hg187242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550901, nsv550902
Samples
Known GenesMBL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1140n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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