A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620823



Internal ID7007693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79263647..79268575hg38UCSC Ensembl
Innerchr9:79263647..79268575hg38UCSC Ensembl
Outerchr9:79263521..79268711hg38UCSC Ensembl
chr9:81878562..81883490hg19UCSC Ensembl
Innerchr9:81878562..81883490hg19UCSC Ensembl
Outerchr9:81878436..81883626hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg384929
hg194929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13534721
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620823
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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