A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598085



Internal ID16385494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50110886..50143556hg38UCSC Ensembl
Innerchr5:49406720..49439390hg19UCSC Ensembl
Innerchr5:49442477..49475147hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3832671
hg1932671
hg1832671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9767n54
Supporting Variantsnssv1030138
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598085
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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