A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656630



Internal ID9922735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86832396..86839676hg38UCSC Ensembl
Outerchr9:86832239..86839829hg38UCSC Ensembl
Innerchr9:89447311..89454591hg19UCSC Ensembl
Outerchr9:89447154..89454744hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387591
hg197591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5883467, essv6245049, essv6164815, essv6307148
SamplesHG00361, HG00182, HG00254, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656630
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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