A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054110



Internal ID18796641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133294417..133352092hg38UCSC Ensembl
Innerchr11:133164312..133221987hg19UCSC Ensembl
Innerchr11:132669522..132727197hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3857676
hg1957676
hg1857676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516512
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054110
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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