A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060398



Internal ID19149617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40846466..40886249hg38UCSC Ensembl
Innerchr19:41352371..41392154hg19UCSC Ensembl
Innerchr19:46044211..46083994hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3839784
hg1939784
hg1839784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3539n100
Supporting Variantsnssv3569426
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060398
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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