A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14004618



Internal ID2000456
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625241
Supporting Variants
SamplesHG01851
Known GenesTRIM34, TRIM6-TRIM34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14004618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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