A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705170



Internal ID15095136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248098027..248252360hg38UCSC Ensembl
Innerchr1:248261329..248415662hg19UCSC Ensembl
Innerchr1:246327952..246482285hg18UCSC Ensembl
Innerchr1:244587370..244741703hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38154334
hg19154334
hg18154334
hg17154334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515858
Supporting Variants
Samples
Known GenesOR2L13, OR2M1P, OR2M2, OR2M3, OR2M4, OR2M5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705170
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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