A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518239



Internal ID15445532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65972842..66025483hg38UCSC Ensembl
Innerchr5:65268670..65321311hg19UCSC Ensembl
Innerchr5:65304426..65357067hg18UCSC Ensembl
Innerchr5:65304426..65357067hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3852642
hg1952642
hg1852642
hg1752642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695671
Samples
Known GenesERBB2IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518239
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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