A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv71n21



Internal ID20131792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58786298..58864895hg38UCSC Ensembl
chr11:58553771..58632368hg19UCSC Ensembl
chr11:58310347..58388944hg18UCSC Ensembl
chr11:58310347..58388944hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3878598
hg1978598
hg1878598
hg1778598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523481, nsv525355
Samples
Known GenesGLYATL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv71n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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