A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620799



Internal ID7007669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78547481..78553545hg38UCSC Ensembl
chr9:81162397..81168461hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1487e214
Supporting Variantsessv13532967, essv13532969, essv13532968
SamplesNA18525, HG01798, HG01799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620799
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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