A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788809



Internal ID18829355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26076885..26183674hg38UCSC Ensembl
Innerchr7:26116505..26223294hg19UCSC Ensembl
Innerchr7:26083030..26189819hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38106790
hg19106790
hg18106790
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891090
Supporting Variants
Samples
Known GenesNFE2L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788809
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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