A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592768



Internal ID16380177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647176..189650466hg38UCSC Ensembl
Innerchr3:189364965..189368255hg19UCSC Ensembl
Innerchr3:190847659..190850949hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg383291
hg193291
hg183291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8779n54
Supporting Variantsnssv982931, nssv982949, nssv982934, nssv982952, nssv982944, nssv982926, nssv982954, nssv982948, nssv982932, nssv982953, nssv982935, nssv982933, nssv982943, nssv982937, nssv982929, nssv982936, nssv982946, nssv982940, nssv982947, nssv982928, nssv982927, nssv982945, nssv982925, nssv982938, nssv982951, nssv982939, nssv982950, nssv982942, nssv982941, nssv982930
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592768
Frequency
Sample Size17421
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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