A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625239



Internal ID6665387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5605080..5678270hg38UCSC Ensembl
chr11:5626310..5699500hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3873191
hg1973191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14003850
SamplesHG01851
Known GenesTRIM34, TRIM5, TRIM6, TRIM6-TRIM34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625239
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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