A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891224



Internal ID19185620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144080902..144177097hg38UCSC Ensembl
Outerchr7:144080902..144177097hg38UCSC Ensembl
Innerchr7:143777995..143874190hg19UCSC Ensembl
Outerchr7:143777995..143874190hg19UCSC Ensembl
Innerchr7:143408928..143505123hg18UCSC Ensembl
Outerchr7:143408928..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3896196
hg1996196
hg1896196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780326
Samples
Known GenesOR2A12, OR2A14, OR2A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891224
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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