A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv55n21



Internal ID22766247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4455469..4518847hg38UCSC Ensembl
chr11:4476699..4540077hg19UCSC Ensembl
chr11:4433275..4496653hg18UCSC Ensembl
chr11:4433275..4496653hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863379
hg1963379
hg1863379
hg1763379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523709, nsv521561
Samples
Known GenesOR52K1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv55n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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