A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679877



Internal ID15069843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18146261..19020595hg38UCSC Ensembl
Innerchr22:18629028..19008108hg19UCSC Ensembl
Innerchr22:17009028..17388108hg18UCSC Ensembl
Innerchr22:17003582..17382662hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38874335
hg19379081
hg18379081
hg17379081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516997
Supporting Variants
Samples
Known GenesDGCR5, DGCR6, DGCR9, GGT3P, PRODH, USP18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679877
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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