A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621631



Internal ID7008499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118986496..118989461hg38UCSC Ensembl
Innerchr9:118986496..118989461hg38UCSC Ensembl
Outerchr9:118986386..118989532hg38UCSC Ensembl
chr9:121748774..121751739hg19UCSC Ensembl
Innerchr9:121748774..121751739hg19UCSC Ensembl
Outerchr9:121748664..121751810hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13612844, essv13612843
SamplesHG00525, HG00473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621631
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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