A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619140



Internal ID7006020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144745609..144765899hg38UCSC Ensembl
chr8:145970994..145991284hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3820291
hg1920291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13369147
SamplesHG01188
Known GenesZNF251
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619140
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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