A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621024



Internal ID7007894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89303699..89307870hg38UCSC Ensembl
Innerchr9:89303699..89307870hg38UCSC Ensembl
Outerchr9:89303430..89308143hg38UCSC Ensembl
chr9:91918614..91922785hg19UCSC Ensembl
Innerchr9:91918614..91922785hg19UCSC Ensembl
Outerchr9:91918345..91923058hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384172
hg194172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549700
SamplesHG03709
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621024
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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