A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058732



Internal ID19147951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40828821..40863082hg38UCSC Ensembl
Innerchr19:41334726..41368987hg19UCSC Ensembl
Innerchr19:46026566..46060827hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3834262
hg1934262
hg1834262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3531n100
Supporting Variantsnssv3568221
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)nsv1058732
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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