A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520472



Internal ID15447765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42746942..42761318hg38UCSC Ensembl
Innerchr22:43142948..43157324hg19UCSC Ensembl
Innerchr22:41472892..41487268hg18UCSC Ensembl
Innerchr22:41467446..41481822hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3814377
hg1914377
hg1814377
hg1714377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697441
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520472
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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