A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678283



Internal ID9597702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:167014388..167014481hg38UCSC Ensembl
Innerchr5:166441393..166441486hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5853549
SamplesNA18856
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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