A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5599860



Internal ID9342387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24991340..24993658hg38UCSC Ensembl
chr4:24992962..24995280hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382319
hg192319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666939
Supporting Variants
SamplesNA18539
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5599860
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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