A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891223



Internal ID18838933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143878890..144177097hg38UCSC Ensembl
Outerchr7:143878890..144177097hg38UCSC Ensembl
Innerchr7:143575983..143874190hg19UCSC Ensembl
Outerchr7:143575983..143874190hg19UCSC Ensembl
Innerchr7:143206916..143505123hg18UCSC Ensembl
Outerchr7:143206916..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38298208
hg19298208
hg18298208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779513
Samples
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891223
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer