A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780082



Internal ID18826609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3184567..3344389hg38UCSC Ensembl
Innerchr17:3087861..3247683hg19UCSC Ensembl
Innerchr17:3034611..3194433hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38159823
hg19159823
hg18159823
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892949
Supporting Variants
Samples
Known GenesOR1A1, OR1A2, OR1D4, OR3A1, OR3A2, OR3A4P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780082
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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