A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551954



Internal ID15992677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94645572..94761492hg38UCSC Ensembl
Innerchr10:96405329..96521249hg19UCSC Ensembl
Innerchr10:96395319..96511239hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38115921
hg19115921
hg18115921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv755894, nssv755895
Samples
Known GenesCYP2C18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551954
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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