A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987437



Internal ID16281393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:818810..868368hg38UCSC Ensembl
Innerchr4:812598..862156hg19UCSC Ensembl
Innerchr4:802598..852156hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849559
hg1949559
hg1849559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593224
Supporting Variants
Samples
Known GenesCPLX1, GAK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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