A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573759



Internal ID16014482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830015..89832059hg38UCSC Ensembl
Innerchr16:89896423..89898467hg19UCSC Ensembl
Innerchr16:88423924..88425968hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382045
hg192045
hg182045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5327n54
Supporting Variantsnssv863512, nssv863514, nssv863511, nssv863513
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573759
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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