A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596855



Internal ID16037578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1370717..1394407hg38UCSC Ensembl
Innerchr5:1370832..1394522hg19UCSC Ensembl
Innerchr5:1423832..1447522hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3823691
hg1923691
hg1823691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9535n54
Supporting Variantsnssv1153521
SamplesHGDP00971
Known GenesSLC6A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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