A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660894



Internal ID15397546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669207..15718554hg38UCSC Ensembl
Innerchr19:15780017..15829364hg19UCSC Ensembl
Innerchr19:15641017..15690364hg18UCSC Ensembl
Innerchr19:15641017..15690364hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3849348
hg1949348
hg1849348
hg1749348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516707
Supporting Variants
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660894
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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