A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780326



Internal ID19172288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144080902..144177097hg38UCSC Ensembl
Innerchr7:143777995..143874190hg19UCSC Ensembl
Innerchr7:143408928..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3896196
hg1996196
hg1896196
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891224
Supporting Variants
Samples
Known GenesOR2A12, OR2A14, OR2A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780326
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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