A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676045



Internal ID15066011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:11305872..11323791hg38UCSC Ensembl
Innerchr12:11458806..11476725hg19UCSC Ensembl
Innerchr12:11350073..11367992hg18UCSC Ensembl
Innerchr12:11350073..11367992hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3817920
hg1917920
hg1817920
hg1717920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516262
Supporting Variants
Samples
Known GenesPRB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676045
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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