A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657387



Internal ID9923492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81009148..81017782hg38UCSC Ensembl
Outerchr9:81008991..81017935hg38UCSC Ensembl
Innerchr9:83624063..83632697hg19UCSC Ensembl
Outerchr9:83623906..83632850hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg388945
hg198945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6349680
SamplesHG00654
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657387
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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