A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596694



Internal ID16384103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:474507..487159hg38UCSC Ensembl
Innerchr5:474622..487274hg19UCSC Ensembl
Innerchr5:527622..540274hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3812653
hg1912653
hg1812653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9493n54
Supporting Variantsnssv1021252
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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