A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686629



Internal ID15076595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161541303..161668596hg38UCSC Ensembl
Innerchr1:161511093..161638386hg19UCSC Ensembl
Innerchr1:159777717..159905010hg18UCSC Ensembl
Innerchr1:158324148..158370058hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38127294
hg19127294
hg18127294
hg1745911
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)nssv686629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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