A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518862



Internal ID15099469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7887365..7896398hg38UCSC Ensembl
Innerchr5:7887478..7896511hg19UCSC Ensembl
Innerchr5:7940478..7949511hg18UCSC Ensembl
Innerchr5:7940478..7949511hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389034
hg199034
hg189034
hg179034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv334n21
Supporting Variantsnssv696317
Samples
Known GenesMTRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518862
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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