A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598838



Internal ID16386247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86322885..86397372hg38UCSC Ensembl
Innerchr5:85618703..85693190hg19UCSC Ensembl
Innerchr5:85654459..85728946hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3874488
hg1974488
hg1874488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1035786
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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