A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989943



Internal ID7061186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374481..39528780hg38UCSC Ensembl
Innerchr8:39232000..39386299hg19UCSC Ensembl
Innerchr8:39351157..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 Variantsdgv181e180
Supporting Variantsessv3587025
SamplesHuRef
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989943
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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