A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600031



Internal ID16040754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151411622..151412762hg38UCSC Ensembl
Innerchr5:150791183..150792323hg19UCSC Ensembl
Innerchr5:150771376..150772516hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381141
hg191141
hg181141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10126n54
Supporting Variantsnssv1043705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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