A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616072



Internal ID7002959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6178075..6381571hg38UCSC Ensembl
chr8:6035596..6239092hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38203497
hg19203497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13078795, essv13078794, essv13078796
SamplesHG00114, HG00116, HG03432
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616072
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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