A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579555



Internal ID16366964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850094..40878673hg38UCSC Ensembl
Innerchr19:41355999..41384578hg19UCSC Ensembl
Innerchr19:46047839..46076418hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3828580
hg1928580
hg1828580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6446n54
Supporting Variantsnssv899451, nssv899441, nssv899447, nssv899440, nssv899449, nssv899448, nssv899445, nssv899450, nssv899438, nssv899444, nssv899442, nssv899443, nssv899439, nssv899446
Samples
Known GenesCYP2A6, CYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579555
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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