A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056515



Internal ID19145734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40845091..40864876hg38UCSC Ensembl
Innerchr19:41350996..41370781hg19UCSC Ensembl
Innerchr19:46042836..46062621hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3819786
hg1919786
hg1819786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3537n100
Supporting Variantsnssv3724549, nssv3568271
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056515
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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