A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv79n21



Internal ID20131800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93497971..93507681hg38UCSC Ensembl
chr11:93231137..93240847hg19UCSC Ensembl
chr11:92870785..92880495hg18UCSC Ensembl
chr11:92870785..92880495hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389711
hg199711
hg189711
hg179711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522568, nsv516461
Samples
Known GenesSMCO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv79n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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