A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891874



Internal ID19186270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81708902..81749799hg38UCSC Ensembl
Outerchr10:81708902..81749799hg38UCSC Ensembl
Innerchr10:83468658..83509555hg19UCSC Ensembl
Outerchr10:83468658..83509555hg19UCSC Ensembl
Innerchr10:83458638..83499535hg18UCSC Ensembl
Outerchr10:83458638..83499535hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3840898
hg1940898
hg1840898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798974
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891874
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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