A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693890



Internal ID15083856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161548967..161677017hg38UCSC Ensembl
Innerchr1:161518757..161646807hg19UCSC Ensembl
Innerchr1:159785381..159913431hg18UCSC Ensembl
Innerchr1:158331812..158378474hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38128051
hg19128051
hg18128051
hg1746663
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
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693890
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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