A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621348



Internal ID7008217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104974916..104992138hg38UCSC Ensembl
Innerchr9:104975416..104991638hg38UCSC Ensembl
Outerchr9:104973916..104993138hg38UCSC Ensembl
chr9:107737197..107754419hg19UCSC Ensembl
Innerchr9:107737697..107753919hg19UCSC Ensembl
Outerchr9:107736197..107755419hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3817223
hg1917223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1499e214
Supporting Variantsessv13592542, essv13592540, essv13592541
SamplesHG01506, HG03681, HG03698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621348
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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