A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050579



Internal ID19139798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122684157..122728417hg38UCSC Ensembl
Innerchr11:122554865..122599125hg19UCSC Ensembl
Innerchr11:122060075..122104335hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3844261
hg1944261
hg1844261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710761
Samples
Known GenesUBASH3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050579
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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