A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586041



Internal ID7057423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375220..39520881hg38UCSC Ensembl
Innerchr8:39232739..39378400hg19UCSC Ensembl
Innerchr8:39351896..39497557hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38145662
hg19145662
hg18145662
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994002
Supporting Variants
SamplesHuRef
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586041
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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