A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058747



Internal ID19147966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40828821..40870102hg38UCSC Ensembl
Innerchr19:41334726..41376007hg19UCSC Ensembl
Innerchr19:46026566..46067847hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3841282
hg1941282
hg1841282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3531n100
Supporting Variantsnssv3568222
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058747
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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