A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569778



Internal ID18868059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15688466..15714929hg38UCSC Ensembl
Innerchr19:15799276..15825739hg19UCSC Ensembl
Innerchr19:15660276..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3826464
hg1926464
hg1826464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062293
Supporting Variants
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3569778
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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