A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1302n100



Internal ID20152918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134275705..134348093hg38UCSC Ensembl
chr11:134145599..134217987hg19UCSC Ensembl
chr11:133650809..133723197hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3872389
hg1972389
hg1872389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037187, nsv1043267, nsv1040950, nsv1046792, nsv1052781, nsv1035257, nsv1038713, nsv1049321, nsv1053506
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)dgv1302n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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