A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522282



Internal ID15449575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142087361..142088689hg38UCSC Ensembl
Innerchr5:141466926..141468254hg19UCSC Ensembl
Innerchr5:141447110..141448438hg18UCSC Ensembl
Innerchr5:141447110..141448438hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381329
hg191329
hg181329
hg171329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695065
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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