A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661574



Internal ID9927679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64724221..65207410hg38UCSC Ensembl
Outerchr9:64724187..65207445hg38UCSC Ensembl
Innerchr9:69736639..70101016hg19UCSC Ensembl
Outerchr9:69736605..70101051hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38483259
hg19364447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1350e199
Supporting Variantsessv5782842
SamplesHG00190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661574
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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