A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587006



Internal ID6711702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102227733..102228274hg38UCSC Ensembl
Innerchr10:103987490..103988031hg19UCSC Ensembl
Innerchr10:103977480..103978021hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38542
hg19542
hg18542
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997610
Supporting Variants
SamplesHuRef
Known GenesELOVL3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587006
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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