A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519472



Internal ID15100079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26458475..26463976hg38UCSC Ensembl
Innerchr22:26854441..26859942hg19UCSC Ensembl
Innerchr22:25184441..25189942hg18UCSC Ensembl
Innerchr22:25178995..25184496hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg385502
hg195502
hg185502
hg175502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696871
Samples
Known GenesHPS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519472
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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