A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2111n54



Internal ID22770006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98585755..98612472hg38UCSC Ensembl
chr11:98456485..98483202hg19UCSC Ensembl
chr11:97961695..97988412hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3826718
hg1926718
hg1826718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556027, nsv556028, nsv556029
Samples1780854293_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2111n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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