A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669766



Internal ID9935871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158217322..158228242hg38UCSC Ensembl
chr5:157644330..157655250hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3810921
hg1910921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6249841, essv6230332
SamplesHG01048, HG01107
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669766
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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