A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620972



Internal ID7007842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86921072..86927857hg38UCSC Ensembl
chr9:89535987..89542772hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386786
hg196786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13546984, essv13546981, essv13546982, essv13546983
SamplesHG03897, HG03888, HG02546, HG01082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620972
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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