A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525270



Internal ID15452563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:43373865..43383861hg38UCSC Ensembl
Innerchr22:43769871..43779867hg19UCSC Ensembl
Innerchr22:42099815..42109811hg18UCSC Ensembl
Innerchr22:42094369..42104365hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg389997
hg199997
hg189997
hg179997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701370
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525270
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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