A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066009



Internal ID19155228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40854226..40886980hg38UCSC Ensembl
Innerchr19:41360131..41392885hg19UCSC Ensembl
Innerchr19:46051971..46084725hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3832755
hg1932755
hg1832755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3539n100
Supporting Variantsnssv3725724, nssv3567359
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066009
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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