A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598828



Internal ID16386237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85310710..85393963hg38UCSC Ensembl
Innerchr5:84606528..84689781hg19UCSC Ensembl
Innerchr5:84642284..84725537hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3883254
hg1983254
hg1883254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1035776
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598828
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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