A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039908



Internal ID18782439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121034184..121066198hg38UCSC Ensembl
Innerchr11:120904893..120936907hg19UCSC Ensembl
Innerchr11:120410103..120442117hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832015
hg1932015
hg1832015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509661
Samples
Known GenesTBCEL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039908
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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