A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059413



Internal ID18801944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3365789..3453922hg38UCSC Ensembl
Innerchr17:3269083..3357216hg19UCSC Ensembl
Innerchr17:3215833..3303966hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3888134
hg1988134
hg1888134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719142
Samples
Known GenesOR1E1, OR1E2, OR3A3, SPATA22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059413
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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