A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579574



Internal ID16366983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850846..40877923hg38UCSC Ensembl
Innerchr19:41356751..41383828hg19UCSC Ensembl
Innerchr19:46048591..46075668hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3827078
hg1927078
hg1827078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6446n54
Supporting Variantsnssv899482
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer