A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666844



Internal ID15056810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161541303..161647726hg38UCSC Ensembl
Innerchr1:161511093..161617516hg19UCSC Ensembl
Innerchr1:159777717..159884140hg18UCSC Ensembl
Innerchr1:158324148..158349210hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38106424
hg19106424
hg18106424
hg1725063
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv666844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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