A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv956n100



Internal ID20152572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94657052..94726747hg38UCSC Ensembl
chr10:96416809..96486504hg19UCSC Ensembl
chr10:96406799..96476494hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3869696
hg1969696
hg1869696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043604, nsv1049341
Samples
Known GenesCYP2C18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv956n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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