A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661755



Internal ID9927860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140624539..140626595hg38UCSC Ensembl
chr5:140004124..140006180hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382057
hg192057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1042e199
Supporting Variantsessv6312115
SamplesNA12341
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661755
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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