A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798654



Internal ID18816254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102487446..102654790hg38UCSC Ensembl
Innerchr7:102127893..102295237hg19UCSC Ensembl
Innerchr7:101914898..102082473hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38167345
hg19167345
hg18167576
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891168
Supporting Variants
Samples
Known GenesPOLR2J2, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B, UPK3BL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798654
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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