A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579558



Internal ID16366967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850149..40873243hg38UCSC Ensembl
Innerchr19:41356054..41379148hg19UCSC Ensembl
Innerchr19:46047894..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823095
hg1923095
hg1823095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6446n54
Supporting Variantsnssv899457, nssv899456, nssv899458
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579558
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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