A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv58n21



Internal ID20131779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7652157..7688219hg38UCSC Ensembl
chr11:7673388..7709450hg19UCSC Ensembl
chr11:7629964..7666026hg18UCSC Ensembl
chr11:7629964..7666026hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3836063
hg1936063
hg1836063
hg1736063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519594, nsv524361
Samples
Known GenesCYB5R2, PPFIBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv58n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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