A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596877



Internal ID16384286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1497511..1514347hg38UCSC Ensembl
Innerchr5:1497626..1514462hg19UCSC Ensembl
Innerchr5:1550626..1567462hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3816837
hg1916837
hg1816837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1022174
Samples
Known GenesLPCAT1, MIR6075
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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