A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv957n100



Internal ID19011325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94735420..94805859hg38UCSC Ensembl
chr10:96495177..96565616hg19UCSC Ensembl
chr10:96485167..96555606hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3870440
hg1970440
hg1870440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049558, nsv1046919, nsv1039270, nsv1044621
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)dgv957n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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