A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv77n21



Internal ID22766269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88453960..88465762hg38UCSC Ensembl
chr11:88187128..88198930hg19UCSC Ensembl
chr11:87826776..87838578hg18UCSC Ensembl
chr11:87826776..87838578hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3811803
hg1911803
hg1811803
hg1711803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528117, nsv523026
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv77n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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