A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618856



Internal ID7005738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131648971..131719766hg38UCSC Ensembl
chr8:132661218..132732013hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3870796
hg1970796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1419e214
Supporting Variantsessv13333944, essv13333943
SamplesNA20294, NA19921
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618856
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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