A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621836



Internal ID7008702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129590508..129592862hg38UCSC Ensembl
Innerchr9:129590508..129592862hg38UCSC Ensembl
Outerchr9:129590327..129593144hg38UCSC Ensembl
chr9:132352787..132355141hg19UCSC Ensembl
Innerchr9:132352787..132355141hg19UCSC Ensembl
Outerchr9:132352606..132355423hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382355
hg192355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628399, essv13628397, essv13628398
SamplesHG01188, HG01064, HG02570
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621836
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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