A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892949



Internal ID18837083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3190584..3344358hg38UCSC Ensembl
Outerchr17:3184567..3344389hg38UCSC Ensembl
Innerchr17:3093878..3247652hg19UCSC Ensembl
Outerchr17:3087861..3247683hg19UCSC Ensembl
Innerchr17:3040628..3194402hg18UCSC Ensembl
Outerchr17:3034611..3194433hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38159823
hg19159823
hg18159823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780082, essv25796676
Samples
Known GenesOR1A1, OR1A2, OR1D4, OR3A1, OR3A2, OR3A4P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892949
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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