A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589107



Internal ID16376516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44614111..44644418hg38UCSC Ensembl
Innerchr22:45009991..45040298hg19UCSC Ensembl
Innerchr22:43388655..43418962hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3830308
hg1930308
hg1830308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957187
Samples
Known GenesLINC00229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589107
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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