A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618775



Internal ID7005657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127484802..127518472hg38UCSC Ensembl
chr8:128497047..128530717hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3833671
hg1933671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1418e214
Supporting Variantsessv13322218, essv13322220, essv13322219
SamplesNA19435, HG03488, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618775
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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