A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12256n54



Internal ID22780151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107492679..107496888hg38UCSC Ensembl
chr8:108504907..108509116hg19UCSC Ensembl
chr8:108574083..108578292hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg384210
hg194210
hg184210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611861, nsv611869, nsv611866
Samples
Known GenesANGPT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12256n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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