A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049225



Internal ID18791756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94645745..94757047hg38UCSC Ensembl
Innerchr10:96405502..96516804hg19UCSC Ensembl
Innerchr10:96395492..96506794hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38111303
hg19111303
hg18111303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv955n100
Supporting Variantsnssv3515739
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)nsv1049225
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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