A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526738



Internal ID15454031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47275457..47291868hg38UCSC Ensembl
Innerchr22:47671207..47687618hg19UCSC Ensembl
Innerchr22:46049871..46066282hg18UCSC Ensembl
Innerchr22:45991726..46008137hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3816412
hg1916412
hg1816412
hg1716412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv264n21
Supporting Variantsnssv703081
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526738
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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