A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551962



Internal ID15992685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94920508..94974582hg38UCSC Ensembl
Innerchr10:96680265..96734339hg19UCSC Ensembl
Innerchr10:96670255..96724329hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3854075
hg1954075
hg1854075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv755905
Samples
Known GenesCYP2C9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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