A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797733



Internal ID18828771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86573217..86589781hg38UCSC Ensembl
Innerchr10:88332974..88349538hg19UCSC Ensembl
Innerchr10:88322954..88339518hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3816565
hg1916565
hg1816565
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891879
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797733
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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