A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625241



Internal ID6665389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5618277..5657863hg38UCSC Ensembl
Innerchr11:5618277..5657863hg38UCSC Ensembl
Outerchr11:5617777..5658363hg38UCSC Ensembl
chr11:5639507..5679093hg19UCSC Ensembl
Innerchr11:5639507..5679093hg19UCSC Ensembl
Outerchr11:5639007..5679593hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3839587
hg1939587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14004618
SamplesHG01851
Known GenesTRIM34, TRIM6-TRIM34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625241
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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