A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568627



Internal ID18520222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669805..15714929hg38UCSC Ensembl
Innerchr19:15780615..15825739hg19UCSC Ensembl
Innerchr19:15641615..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3845125
hg1945125
hg1845125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063313
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)nssv3568627
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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