A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599099



Internal ID16386508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99009478..99021029hg38UCSC Ensembl
Innerchr5:98345182..98356733hg19UCSC Ensembl
Innerchr5:98373082..98384633hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3811552
hg1911552
hg1811552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9960n54
Supporting Variantsnssv1039446, nssv1039441, nssv1039448, nssv1039440, nssv1039447, nssv1039444, nssv1039445, nssv1039443, nssv1039442
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599099
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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