A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6175679



Internal ID9153082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125205501..125215741hg38UCSC Ensembl
chr11:125075397..125085637hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810241
hg1910241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659940
Supporting Variants
SamplesHG00117
Known GenesPKNOX2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6175679
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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