A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674472



Internal ID9940577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162275624..162280946hg38UCSC Ensembl
chr5:161702630..161707952hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385323
hg195323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5441777
SamplesNA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674472
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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