A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv66n21



Internal ID18990539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43538441..43560642hg38UCSC Ensembl
chr11:43559991..43582192hg19UCSC Ensembl
chr11:43516567..43538768hg18UCSC Ensembl
chr11:43516567..43538768hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3822202
hg1922202
hg1822202
hg1722202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524728, nsv522547
Samples
Known GenesMIR670
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv66n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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