A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669157



Internal ID15059123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45362878..45378388hg38UCSC Ensembl
Innerchr22:45758758..45774268hg19UCSC Ensembl
Innerchr22:44137422..44152932hg18UCSC Ensembl
Innerchr22:44079295..44094805hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3815511
hg1915511
hg1815511
hg1715511
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)nssv669157
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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