A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522232



Internal ID15449525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125985204..125998274hg38UCSC Ensembl
Innerchr12:126469750..126482820hg19UCSC Ensembl
Innerchr12:125035703..125048773hg18UCSC Ensembl
Innerchr12:124994630..125007700hg17UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3813071
hg1913071
hg1813071
hg1713071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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