A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506659



Internal ID18458254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:1968731..2020607hg38UCSC Ensembl
Innerchr12:2077897..2129773hg19UCSC Ensembl
Innerchr12:1948158..2000034hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3851877
hg1951877
hg1851877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042378
Supporting Variants
Samples
Known GenesDCP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506659
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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