A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044621



Internal ID19133840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94735420..94786778hg38UCSC Ensembl
Innerchr10:96495177..96546535hg19UCSC Ensembl
Innerchr10:96485167..96536525hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3851359
hg1951359
hg1851359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv957n100
Supporting Variantsnssv3706195
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044621
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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