A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672969



Internal ID9939074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33376745..33378911hg38UCSC Ensembl
Outerchr9:33376708..33378961hg38UCSC Ensembl
Innerchr9:33376743..33378909hg19UCSC Ensembl
Outerchr9:33376706..33378959hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382254
hg192254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6242775
SamplesHG00701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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