A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659004



Internal ID9925109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:89594181..89594453hg38UCSC Ensembl
Outerchr5:89594133..89594503hg38UCSC Ensembl
Innerchr5:88889998..88890270hg19UCSC Ensembl
Outerchr5:88889950..88890320hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5916102
SamplesNA11994
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659004
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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