A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660853



Internal ID9926958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76369656..76371235hg38UCSC Ensembl
chr5:75665481..75667060hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5637623
SamplesHG01055
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660853
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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