A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677518



Internal ID15414170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161530340..161677017hg38UCSC Ensembl
Innerchr1:161500130..161646807hg19UCSC Ensembl
Innerchr1:159766754..159913431hg18UCSC Ensembl
Innerchr1:158313185..158378474hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38146678
hg19146678
hg18146678
hg1765290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517640
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677518
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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