A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12105n54



Internal ID22780000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39444480..39541538hg38UCSC Ensembl
chr8:39301999..39399057hg19UCSC Ensembl
chr8:39421156..39518214hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3897059
hg1997059
hg1897059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611052, nsv611060
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12105n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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