A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526125



Internal ID15453418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:116698982..116701027hg38UCSC Ensembl
Innerchr12:117136787..117138832hg19UCSC Ensembl
Innerchr12:115621170..115623215hg18UCSC Ensembl
Innerchr12:115599507..115601552hg17UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg382046
hg192046
hg182046
hg172046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702376
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526125
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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