A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598836



Internal ID16386245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86310631..86358387hg38UCSC Ensembl
Innerchr5:85606449..85654205hg19UCSC Ensembl
Innerchr5:85642205..85689961hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3847757
hg1947757
hg1847757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9919n54
Supporting Variantsnssv1035785
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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