A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064179



Internal ID19153398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45741650..45760532hg38UCSC Ensembl
Innerchr22:46137530..46156412hg19UCSC Ensembl
Innerchr22:44516194..44535076hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3818883
hg1918883
hg1818883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3592261
Samples
Known GenesATXN10, MIR4762
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064179
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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