A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598156



Internal ID16385565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52045037..52131895hg38UCSC Ensembl
Innerchr5:51340871..51427729hg19UCSC Ensembl
Innerchr5:51376628..51463486hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3886859
hg1986859
hg1886859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9783n54
Supporting Variantsnssv1030341
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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