A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1159n100



Internal ID22787246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54953335..55172866hg38UCSC Ensembl
chr11:54720811..54940342hg19UCSC Ensembl
chr11:54477387..54696918hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38219532
hg19219532
hg18219532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035974, nsv1041578, nsv1054501, nsv1045742
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1159n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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