A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698701



Internal ID15435353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12520617..12535247hg38UCSC Ensembl
Innerchr12:12673551..12688181hg19UCSC Ensembl
Innerchr12:12564818..12579448hg18UCSC Ensembl
Innerchr12:12564818..12579448hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3814631
hg1914631
hg1814631
hg1714631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523022
Supporting Variants
Samples
Known GenesDUSP16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698701
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