A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665551



Internal ID15055517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:247982342..248114336hg38UCSC Ensembl
Innerchr1:248145644..248277638hg19UCSC Ensembl
Innerchr1:246212267..246344261hg18UCSC Ensembl
Innerchr1:244471685..244603679hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38131995
hg19131995
hg18131995
hg17131995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515858
Supporting Variants
Samples
Known GenesOR2L13, OR2L1P, OR2L2, OR2L3, OR2L5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665551
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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