A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662971



Internal ID9929076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:39077007..39100105hg38UCSC Ensembl
Outerchr5:39076850..39100303hg38UCSC Ensembl
Innerchr5:39077109..39100207hg19UCSC Ensembl
Outerchr5:39076952..39100405hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3823454
hg1923454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5623832
SamplesNA20818
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662971
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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