A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527362



Internal ID15454655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:103635684..103645196hg38UCSC Ensembl
Innerchr12:104029462..104038974hg19UCSC Ensembl
Innerchr12:102553592..102563104hg18UCSC Ensembl
Innerchr12:102531929..102541441hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg389513
hg199513
hg189513
hg179513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703793
Samples
Known GenesSTAB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer