A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1484e214



Internal ID20122907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76784399..76818145hg38UCSC Ensembl
chr9:79399315..79433061hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3833747
hg1933747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620748, esv3620747
SamplesNA19332, HG04094, HG02655, NA19922
Known GenesPCA3, PRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1484e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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