A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657394



Internal ID15047360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31057180..31253875hg38UCSC Ensembl
Innerchr12:31210114..31406809hg19UCSC Ensembl
Innerchr12:31101381..31298076hg18UCSC Ensembl
Innerchr12:31101381..31298076hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38196696
hg19196696
hg18196696
hg17196696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515974
Supporting Variants
Samples
Known GenesDDX11, DDX11-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657394
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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