A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779513



Internal ID18830284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143878890..144177097hg38UCSC Ensembl
Innerchr7:143575983..143874190hg19UCSC Ensembl
Innerchr7:143206916..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38298208
hg19298208
hg18298208
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891223
Supporting Variants
Samples
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=66
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779513
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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