A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674722



Internal ID9940827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92827209..92835939hg38UCSC Ensembl
chr5:92162916..92171646hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg388731
hg198731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5656481
SamplesNA19818
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674722
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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