A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588953



Internal ID16376362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36215260..36218243hg38UCSC Ensembl
Innerchr22:36611306..36614289hg19UCSC Ensembl
Innerchr22:34941252..34944235hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382984
hg192984
hg182984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv955464
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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