A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519779



Internal ID15100386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161509955..161668596hg38UCSC Ensembl
Innerchr1:161479745..161638386hg19UCSC Ensembl
Innerchr1:159746369..159905010hg18UCSC Ensembl
Innerchr1:158292800..158370058hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38158642
hg19158642
hg18158642
hg1777259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697045
Samples
Known GenesFCGR2A, FCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA6, HSPA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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