A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv956721



Internal ID16250677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38776106..38861392hg38UCSC Ensembl
Innerchr22:39172111..39257397hg19UCSC Ensembl
Innerchr22:37502057..37587343hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3885287
hg1985287
hg1885287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589009
Supporting Variants
Samples
Known GenesDNAL4, NPTXR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv956721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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