A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620798



Internal ID7007668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547199..78555379hg38UCSC Ensembl
Innerchr9:78547201..78555378hg38UCSC Ensembl
Outerchr9:78547198..78555381hg38UCSC Ensembl
chr9:81162115..81170295hg19UCSC Ensembl
Innerchr9:81162117..81170294hg19UCSC Ensembl
Outerchr9:81162114..81170297hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg388181
hg198181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1487e214
Supporting Variantsessv13532966, essv13532964, essv13532965
SamplesNA18525, HG01798, HG01799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620798
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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