A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656982



Internal ID9923087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140882391..140888139hg38UCSC Ensembl
Outerchr7:140882354..140888189hg38UCSC Ensembl
Innerchr7:140582191..140587939hg19UCSC Ensembl
Outerchr7:140582154..140587989hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385836
hg195836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5909544
SamplesHG01350
Known GenesBRAF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656982
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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