A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658801



Internal ID9924906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140279386..140280639hg38UCSC Ensembl
Outerchr8:140279349..140280689hg38UCSC Ensembl
Innerchr8:141289485..141290738hg19UCSC Ensembl
Outerchr8:141289448..141290788hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6236851
SamplesNA20819
Known GenesTRAPPC9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658801
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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