A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5971431



Internal ID8948834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131849801..131854667hg38UCSC Ensembl
chr11:131719695..131724561hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384867
hg194867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675610
Supporting Variants
SamplesNA18562
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5971431
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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