A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523629



Internal ID6019648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36679058..36684354hg19UCSC Ensembl
Innerchr22:35009004..35014300hg18UCSC Ensembl
Innerchr22:35003558..35008854hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv699428
Samples
Known GenesMYH9
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv523629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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