A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596691



Internal ID16037414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:474296..492304hg38UCSC Ensembl
Innerchr5:474411..492419hg19UCSC Ensembl
Innerchr5:527411..545419hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3818009
hg1918009
hg1818009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1021249
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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