A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588944



Internal ID16376353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34544950..34611054hg38UCSC Ensembl
Innerchr22:34940942..35007046hg19UCSC Ensembl
Innerchr22:33270942..33337046hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3866105
hg1966105
hg1866105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8092n54
Supporting Variantsnssv954750
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588944
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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