A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597960



Internal ID16385369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45187816..45193367hg38UCSC Ensembl
Innerchr5:45187918..45193469hg19UCSC Ensembl
Innerchr5:45223675..45229226hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg385552
hg195552
hg185552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9743n54
Supporting Variantsnssv1029622
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597960
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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