A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13528559



Internal ID3530375
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620747
Supporting Variants
SamplesHG02655
Known GenesPCA3, PRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13528559
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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