A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798039



Internal ID18815347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1280422..1296827hg38UCSC Ensembl
Innerchr10:1322617..1339022hg19UCSC Ensembl
Innerchr10:1312617..1329022hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3816406
hg1916406
hg1816406
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891738
Supporting Variants
Samples
Known GenesADARB2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798039
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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