A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798974



Internal ID19179444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81708902..81749799hg38UCSC Ensembl
Innerchr10:83468658..83509555hg19UCSC Ensembl
Innerchr10:83458638..83499535hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3840898
hg1940898
hg1840898
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891874
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798974
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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