A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049558



Internal ID19138777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94738127..94798954hg38UCSC Ensembl
Innerchr10:96497884..96558711hg19UCSC Ensembl
Innerchr10:96487874..96548701hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3860828
hg1960828
hg1860828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv957n100
Supporting Variantsnssv3706196
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)nsv1049558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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