A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755898



Internal ID15703168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94694399..94866925hg38UCSC Ensembl
Innerchr10:96454156..96626682hg19UCSC Ensembl
Innerchr10:96444146..96616672hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38172527
hg19172527
hg18172527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551957
Supporting Variants
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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