A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv927n54



Internal ID20134351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1237304..1240333hg38UCSC Ensembl
chr10:1281436..1282372hg19UCSC Ensembl
chr10:1271436..1272372hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383030
hg19937
hg18937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549770, nsv549777, nsv549781, nsv549779, nsv549776
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv927n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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