A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574236



Internal ID16361645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3390044..3459775hg38UCSC Ensembl
Innerchr17:3293338..3363069hg19UCSC Ensembl
Innerchr17:3240088..3309819hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3869732
hg1969732
hg1869732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866447
Samples
Known GenesOR1E1, OR1E2, OR3A3, SPATA22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574236
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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