A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058261



Internal ID18800792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33397437..33427322hg38UCSC Ensembl
Innerchr22:33793423..33823308hg19UCSC Ensembl
Innerchr22:32123423..32153308hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3829886
hg1929886
hg1829886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734202
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058261
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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