A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621020



Internal ID7007890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89212897..89217648hg38UCSC Ensembl
Innerchr9:89212947..89217598hg38UCSC Ensembl
Outerchr9:89212843..89217702hg38UCSC Ensembl
chr9:91827812..91832563hg19UCSC Ensembl
Innerchr9:91827862..91832513hg19UCSC Ensembl
Outerchr9:91827758..91832617hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549696
SamplesHG00171
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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