A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5623832



Internal ID9919671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:39077007..39100105hg38UCSC Ensembl
Outerchr5:39076850..39100303hg38UCSC Ensembl
Innerchr5:39077109..39100207hg19UCSC Ensembl
Outerchr5:39076952..39100405hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3823454
hg1923454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662971
Supporting Variants
SamplesNA20818
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5623832
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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