A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv181e180



Internal ID22757591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374481..39528780hg38UCSC Ensembl
chr8:39232000..39386299hg19UCSC Ensembl
chr8:39351157..39505456hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38154300
hg19154300
hg18154300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv994002, esv989943
SamplesHuRef
Known GenesADAM3A, ADAM5
MethodOligo aCGH
SNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv181e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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