A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1773n54



Internal ID22769668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43984709..43993819hg38UCSC Ensembl
chr11:44006259..44015369hg19UCSC Ensembl
chr11:43962835..43971945hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389111
hg199111
hg189111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554172, nsv554173
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1773n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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