A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701036



Internal ID15437688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:50633733..50639823hg38UCSC Ensembl
Innerchr22:51072161..51078251hg19UCSC Ensembl
Innerchr22:49419027..49425117hg18UCSC Ensembl
Innerchr22:49362305..49368395hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg386091
hg196091
hg186091
hg176091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519694
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701036
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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