A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891879



Internal ID18839589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86573217..86588805hg38UCSC Ensembl
Outerchr10:86573217..86589781hg38UCSC Ensembl
Innerchr10:88332974..88348562hg19UCSC Ensembl
Outerchr10:88332974..88349538hg19UCSC Ensembl
Innerchr10:88322954..88338542hg18UCSC Ensembl
Outerchr10:88322954..88339518hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3816565
hg1916565
hg1816565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797733, essv25782273
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891879
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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