A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527091



Internal ID15107698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3265509..3277848hg38UCSC Ensembl
Innerchr12:3374675..3387014hg19UCSC Ensembl
Innerchr12:3244936..3257275hg18UCSC Ensembl
Innerchr12:3244936..3257275hg17UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3812340
hg1912340
hg1812340
hg1712340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703470
Samples
Known GenesTSPAN9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527091
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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