A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043604



Internal ID18786135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94664636..94726747hg38UCSC Ensembl
Innerchr10:96424393..96486504hg19UCSC Ensembl
Innerchr10:96414383..96476494hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3862112
hg1962112
hg1862112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv956n100
Supporting Variantsnssv3510112
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)nsv1043604
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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