A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668296



Internal ID9934401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153090543..153091757hg38UCSC Ensembl
chr5:152470103..152471317hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5751353
SamplesHG01390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668296
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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