A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564897



Internal ID18516492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15714929hg38UCSC Ensembl
Innerchr19:15780041..15825739hg19UCSC Ensembl
Innerchr19:15641041..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3845699
hg1945699
hg1845699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061202
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)nssv3564897
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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