A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519563



Internal ID15446856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17104551..17108356hg38UCSC Ensembl
Innerchr22:17585441..17589246hg19UCSC Ensembl
Innerchr22:15965441..15969246hg18UCSC Ensembl
Innerchr22:15959995..15963800hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg383806
hg193806
hg183806
hg173806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676115, nssv697900, nssv658434
Samples
Known GenesIL17RA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519563
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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