A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596856



Internal ID16037579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1372589..1394962hg38UCSC Ensembl
Innerchr5:1372704..1395077hg19UCSC Ensembl
Innerchr5:1425704..1448077hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3822374
hg1922374
hg1822374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9535n54
Supporting Variantsnssv1153522
SamplesHGDP00830
Known GenesSLC6A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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