A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611654



Internal ID6651872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167256381..167320502hg38UCSC Ensembl
chr6:167669869..167733990hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864122
hg1964122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643420, essv12643415, essv12643414, essv12643417, essv12643416, essv12643418, essv12643419, essv12643421
SamplesHG02890, HG02610, HG03241, HG03460, HG02571, HG03428, NA20281, HG03401
Known GenesUNC93A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611654
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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