A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656922



Internal ID15046888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45362878..45383455hg38UCSC Ensembl
Innerchr22:45758758..45779335hg19UCSC Ensembl
Innerchr22:44137422..44157999hg18UCSC Ensembl
Innerchr22:44079295..44099872hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3820578
hg1920578
hg1820578
hg1720578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515690
Supporting Variants
Samples
Known GenesSMC1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656922
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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