A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619828



Internal ID7006702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16988089..17064870hg38UCSC Ensembl
Innerchr9:16988089..17064870hg38UCSC Ensembl
Outerchr9:16987994..17064942hg38UCSC Ensembl
chr9:16988087..17064868hg19UCSC Ensembl
Innerchr9:16988087..17064868hg19UCSC Ensembl
Outerchr9:16987992..17064940hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3876782
hg1976782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13411501
SamplesNA20756
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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