A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621092



Internal ID7007962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92907214..92907708hg38UCSC Ensembl
Innerchr9:92907230..92907692hg38UCSC Ensembl
Outerchr9:92907198..92907724hg38UCSC Ensembl
chr9:95669496..95669990hg19UCSC Ensembl
Innerchr9:95669512..95669974hg19UCSC Ensembl
Outerchr9:95669480..95670006hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559503, essv13559501, essv13559506, essv13559509, essv13559495, essv13559502, essv13559511, essv13559499, essv13559496, essv13559507, essv13559493, essv13559500, essv13559510, essv13559497, essv13559512, essv13559498, essv13559508, essv13559505, essv13559494, essv13559504
SamplesHG03800, HG04096, HG03941, HG03772, NA21115, HG03950, HG03640, HG03978, HG03709, HG03861, HG03714, HG04062, HG03871, HG04054, NA21093, HG03615, HG03872, HG03856, HG03698, HG01583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621092
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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