A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621627



Internal ID7008495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118816609..118822086hg38UCSC Ensembl
Innerchr9:118816620..118822076hg38UCSC Ensembl
Outerchr9:118816599..118822097hg38UCSC Ensembl
chr9:121578887..121584364hg19UCSC Ensembl
Innerchr9:121578898..121584354hg19UCSC Ensembl
Outerchr9:121578877..121584375hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385478
hg195478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1507e214
Supporting Variantsessv13612836, essv13612837
SamplesNA19355, NA19038
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621627
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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