A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892950



Internal ID19183770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3131812..3577153hg38UCSC Ensembl
Outerchr17:3131812..3577153hg38UCSC Ensembl
Innerchr17:3035106..3480447hg19UCSC Ensembl
Outerchr17:3035106..3480447hg19UCSC Ensembl
Innerchr17:2981856..3427196hg18UCSC Ensembl
Outerchr17:2981856..3427196hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38445342
hg19445342
hg18445341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782804
Samples
Known GenesASPA, OR1A1, OR1A2, OR1D4, OR1E1, OR1E2, OR3A1, OR3A2, OR3A3, OR3A4P, SPATA22, TRPV1, TRPV3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892950
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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