A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620747



Internal ID6660928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76784399..76812922hg38UCSC Ensembl
chr9:79399315..79427838hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3828524
hg1928524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1484e214
Supporting Variantsessv13528559, essv13528560
SamplesHG04094, HG02655
Known GenesPCA3, PRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620747
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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