A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060727



Internal ID18803258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3045742..3209683hg38UCSC Ensembl
Innerchr17:2949036..3112977hg19UCSC Ensembl
Innerchr17:2895786..3059727hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38163942
hg19163942
hg18163942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3084n100
Supporting Variantsnssv3560086
Samples
Known GenesOR1A2, OR1D2, OR1D5, OR1G1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060727
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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