A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055204



Internal ID19144423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40832930..40863792hg38UCSC Ensembl
Innerchr19:41338835..41369697hg19UCSC Ensembl
Innerchr19:46030675..46061537hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3830863
hg1930863
hg1830863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3531n100
Supporting Variantsnssv3568228, nssv3568229
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)nsv1055204
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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