A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564953



Internal ID18516548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669400..15709516hg38UCSC Ensembl
Innerchr19:15780210..15820326hg19UCSC Ensembl
Innerchr19:15641210..15681326hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3840117
hg1940117
hg1840117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065977
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)nssv3564953
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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