A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599411



Internal ID16386820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113799037..113848514hg38UCSC Ensembl
Innerchr5:113134734..113184211hg19UCSC Ensembl
Innerchr5:113162633..113212110hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3849478
hg1949478
hg1849478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10013n54
Supporting Variantsnssv1153585
SamplesHGDP00808
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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