A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598941



Internal ID16386350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93222263..93260233hg38UCSC Ensembl
Innerchr5:92557969..92595939hg19UCSC Ensembl
Innerchr5:92583725..92621695hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3837971
hg1937971
hg1837971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153049
SamplesHGDP00886
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598941
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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