A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618925



Internal ID7005807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135670205..135709293hg38UCSC Ensembl
chr8:136682448..136721536hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3839089
hg1939089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1421e214
Supporting Variantsessv13339103, essv13339104
SamplesHG01326, HG01183
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618925
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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