A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519878



Internal ID15100485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149408099..149419169hg38UCSC Ensembl
Innerchr5:148787662..148798732hg19UCSC Ensembl
Innerchr5:148767855..148778925hg18UCSC Ensembl
Innerchr5:148767855..148778925hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3811071
hg1911071
hg1811071
hg1711071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697101
Samples
Known GenesMIR143HG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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