A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620746



Internal ID6660927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76782493..76783247hg38UCSC Ensembl
Innerchr9:76782493..76783247hg38UCSC Ensembl
Outerchr9:76782290..76783451hg38UCSC Ensembl
chr9:79397409..79398163hg19UCSC Ensembl
Innerchr9:79397409..79398163hg19UCSC Ensembl
Outerchr9:79397206..79398367hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13528558
SamplesNA19007
Known GenesPCA3, PRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620746
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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