A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596922



Internal ID16384331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3591128..3595864hg38UCSC Ensembl
Innerchr5:3591242..3595978hg19UCSC Ensembl
Innerchr5:3644242..3648978hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384737
hg194737
hg184737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9549n54
Supporting Variantsnssv1023679
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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