A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677746



Internal ID15067712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161541303..161685552hg38UCSC Ensembl
Innerchr1:161511093..161655342hg19UCSC Ensembl
Innerchr1:159777717..159921966hg18UCSC Ensembl
Innerchr1:158324148..158387000hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38144250
hg19144250
hg18144250
hg1762853
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517640
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7, RPL31P11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677746
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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