A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722773



Internal ID19021054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40855177..40886249hg38UCSC Ensembl
Innerchr19:41361082..41392154hg19UCSC Ensembl
Innerchr19:46052922..46083994hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3831073
hg1931073
hg1831073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060679
Supporting Variants
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722773
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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