A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5584928



Internal ID9744393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17093025..17098153hg38UCSC Ensembl
Outerchr5:17092988..17098203hg38UCSC Ensembl
Innerchr5:17093134..17098262hg19UCSC Ensembl
Outerchr5:17093097..17098312hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385216
hg195216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673154
Supporting Variants
SamplesNA19681
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5584928
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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