A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621402



Internal ID7008271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107658710..107673130hg38UCSC Ensembl
Innerchr9:107658746..107673095hg38UCSC Ensembl
Outerchr9:107658675..107673166hg38UCSC Ensembl
chr9:110420991..110435411hg19UCSC Ensembl
Innerchr9:110421027..110435376hg19UCSC Ensembl
Outerchr9:110420956..110435447hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3814421
hg1914421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594412, essv13594414, essv13594413
SamplesNA18504, HG02395, HG02180
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621402
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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