A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1303n100



Internal ID20152919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134280623..134340956hg38UCSC Ensembl
chr11:134150517..134210850hg19UCSC Ensembl
chr11:133655727..133716060hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860334
hg1960334
hg1860334
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042202, nsv1047210
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)dgv1303n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss5
Observed Complex0
Frequencyn/a


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