A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891738



Internal ID18839448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1280422..1296827hg38UCSC Ensembl
Outerchr10:1280422..1301002hg38UCSC Ensembl
Innerchr10:1322617..1339022hg19UCSC Ensembl
Outerchr10:1322617..1343197hg19UCSC Ensembl
Innerchr10:1312617..1329022hg18UCSC Ensembl
Outerchr10:1312617..1333197hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3820581
hg1920581
hg1820581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798039, essv25795983, essv25797118
Samples
Known GenesADARB2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891738
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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