A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005931



Internal ID7071025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39374799..39385209hg38UCSC Ensembl
Innerchr8:39232318..39242728hg19UCSC Ensembl
Innerchr8:39351475..39361885hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3810411
hg1910411
hg1810411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586440
SamplesHuRef
Known GenesADAM5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005931
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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