A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693456



Internal ID15083422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161541303..161654964hg38UCSC Ensembl
Innerchr1:161511093..161624754hg19UCSC Ensembl
Innerchr1:159777717..159891378hg18UCSC Ensembl
Innerchr1:158324148..158356421hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38113662
hg19113662
hg18113662
hg1732274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517640
Supporting Variants
Samples
Known GenesFCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693456
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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