A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6182991



Internal ID9254844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84538496..84542282hg38UCSC Ensembl
Outerchr4:84538459..84542332hg38UCSC Ensembl
Innerchr4:85459649..85463435hg19UCSC Ensembl
Outerchr4:85459612..85463485hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg383874
hg193874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676086
Supporting Variants
SamplesNA12155
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6182991
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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