A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891440



Internal ID18839150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91110980..91171430hg38UCSC Ensembl
Outerchr8:91110980..91171430hg38UCSC Ensembl
Innerchr8:92123208..92183658hg19UCSC Ensembl
Outerchr8:92123208..92183658hg19UCSC Ensembl
Innerchr8:92192384..92252834hg18UCSC Ensembl
Outerchr8:92192384..92252834hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3860451
hg1960451
hg1860451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779168, essv25786963, essv25783973, essv25779494, essv25785041, essv25784457, essv25799431, essv25779450, essv25782611, essv25787222, essv25781830, essv25784314, essv25799784
Samples
Known GenesLRRC69
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891440
Frequency
Sample Size3017
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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