A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526328



Internal ID15106935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21974019..22568655hg38UCSC Ensembl
Innerchr22:22328391..22911060hg19UCSC Ensembl
Innerchr22:20658391..21241060hg18UCSC Ensembl
Innerchr22:20652945..21235614hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38594637
hg19582670
hg18582670
hg17582670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702618
Samples
Known GenesBMS1P20, LOC648691, PRAME, TOP3B, VPREB1, ZNF280A, ZNF280B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526328
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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