A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598826



Internal ID16386235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85118019..85174861hg38UCSC Ensembl
Innerchr5:84413837..84470679hg19UCSC Ensembl
Innerchr5:84449593..84506435hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3856843
hg1956843
hg1856843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153960
SamplesHGDP00171
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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