A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523911



Internal ID8418186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36279104..36302946hg38UCSC Ensembl
Innerchr22:36675150..36698992hg19UCSC Ensembl
Innerchr22:35005096..35028938hg18UCSC Ensembl
Innerchr22:34999650..35023492hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3823843
hg1923843
hg1823843
hg1723843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699754
Samples
Known GenesMIR6819, MYH9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523911
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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