A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670057



Internal ID9936162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180582735..180588256hg38UCSC Ensembl
Outerchr5:180582698..180588306hg38UCSC Ensembl
Innerchr5:180009735..180015256hg19UCSC Ensembl
Outerchr5:180009698..180015306hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385609
hg195609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5500111
SamplesNA19079
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670057
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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