A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063079



Internal ID19152298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34794049..34829522hg38UCSC Ensembl
Innerchr22:35190040..35225513hg19UCSC Ensembl
Innerchr22:33520040..33555513hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3835474
hg1935474
hg1835474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734207
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063079
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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