A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063313



Internal ID18805844
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 StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3568631, nssv3568623, nssv3568622, nssv3568629, nssv3568626, nssv3568624, nssv3568625, nssv3568628, nssv3568630, nssv3568627
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)nsv1063313
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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