A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051069



Internal ID18793600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134294724..134340956hg38UCSC Ensembl
Innerchr11:134164618..134210850hg19UCSC Ensembl
Innerchr11:133669828..133716060hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3846233
hg1946233
hg1846233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513525
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051069
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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