A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616079



Internal ID7002966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6262960..6405804hg38UCSC Ensembl
chr8:6120481..6263325hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38142845
hg19142845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13080308, essv13080309, essv13080311, essv13080310
SamplesNA12812, HG01796, HG03432, HG01254
Known GenesLOC100287015
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616079
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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