A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611659



Internal ID6651877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167323380..167358297hg38UCSC Ensembl
chr6:167736868..167771785hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3834918
hg1934918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643447, essv12643444, essv12643443, essv12643446, essv12643448, essv12643449, essv12643445
SamplesHG02890, HG03279, HG03401, HG03241, HG03428, HG02571, HG03460
Known GenesTTLL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611659
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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