A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619996



Internal ID7006869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22784122..22858783hg38UCSC Ensembl
Innerchr9:22784122..22858783hg38UCSC Ensembl
Outerchr9:22783622..22859283hg38UCSC Ensembl
chr9:22784121..22858782hg19UCSC Ensembl
Innerchr9:22784121..22858782hg19UCSC Ensembl
Outerchr9:22783621..22859282hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3874662
hg1974662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13426179, essv13426180
SamplesHG01840, HG02113
Known GenesFLJ35282
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619996
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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