A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521277



Internal ID15448570
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 StatusM
Merged Variants
Supporting Variantsnssv692294, nssv691624
Samples
Known GenesOR1E1, OR1E2, OR3A3, SPATA22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521277
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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