A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1700n54



Internal ID22769595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24088370..24201455hg38UCSC Ensembl
chr11:24109916..24223001hg19UCSC Ensembl
chr11:24066492..24179577hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38113086
hg19113086
hg18113086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553781, nsv553780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1700n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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