A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv928n54



Internal ID20134352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1237571..1239650hg38UCSC Ensembl
chr10:1281487..1282170hg19UCSC Ensembl
chr10:1271487..1272170hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382080
hg19684
hg18684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv549773, nsv549778, nsv549772
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv928n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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