A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706197



Internal ID18657792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94778325..94882192hg38UCSC Ensembl
Innerchr10:96538082..96641949hg19UCSC Ensembl
Innerchr10:96528072..96631939hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38103868
hg19103868
hg18103868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052578
Supporting Variants
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706197
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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