A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598158



Internal ID16385567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:52071620..52129677hg38UCSC Ensembl
Innerchr5:51367454..51425511hg19UCSC Ensembl
Innerchr5:51403211..51461268hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3858058
hg1958058
hg1858058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9784n54
Supporting Variantsnssv1153933
SamplesNINDS_178
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598158
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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