A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12110n54



Internal ID22780005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39483411..39532700hg38UCSC Ensembl
chr8:39340930..39390219hg19UCSC Ensembl
chr8:39460087..39509376hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3849290
hg1949290
hg1849290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611069, nsv611078, nsv611080, nsv611079, nsv611074, nsv611071, nsv611075, nsv611076, nsv611077, nsv611068
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12110n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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