A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046919



Internal ID19136138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94738127..94799408hg38UCSC Ensembl
Innerchr10:96497884..96559165hg19UCSC Ensembl
Innerchr10:96487874..96549155hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3861282
hg1961282
hg1861282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv957n100
Supporting Variantsnssv3508803, nssv3517661
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046919
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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