A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692294



Internal ID15082260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3390044..3468885hg38UCSC Ensembl
Innerchr17:3293338..3372179hg19UCSC Ensembl
Innerchr17:3240088..3318929hg18UCSC Ensembl
Innerchr17:3240088..3318929hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3878842
hg1978842
hg1878842
hg1778842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521277
Supporting Variants
Samples
Known GenesOR1E1, OR1E2, OR3A3, SPATA22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692294
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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