A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568640



Internal ID18520235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15673306..15713261hg38UCSC Ensembl
Innerchr19:15784116..15824071hg19UCSC Ensembl
Innerchr19:15645116..15685071hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3839956
hg1939956
hg1839956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067246
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)nssv3568640
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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