A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062859



Internal ID19152078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:17067835..17108071hg38UCSC Ensembl
Innerchr22:17548725..17588961hg19UCSC Ensembl
Innerchr22:15928725..15968961hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3840237
hg1940237
hg1840237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731798
Samples
Known GenesIL17RA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062859
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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