A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598824



Internal ID16386233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85068399..85113413hg38UCSC Ensembl
Innerchr5:84364217..84409231hg19UCSC Ensembl
Innerchr5:84399973..84444987hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3845015
hg1945015
hg1845015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153959
SamplesHGDP00634
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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