A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618957



Internal ID7005838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137455205..137570559hg38UCSC Ensembl
chr8:138467448..138582802hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38115355
hg19115355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13343621
SamplesHG02408
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618957
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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