A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596690



Internal ID16384099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:474296..474989hg38UCSC Ensembl
Innerchr5:474411..475104hg19UCSC Ensembl
Innerchr5:527411..528104hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38694
hg19694
hg18694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9492n54
Supporting Variantsnssv1021248
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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