A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5866075



Internal ID8884917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133053728..133090685hg38UCSC Ensembl
Outerchr4:133053691..133090735hg38UCSC Ensembl
Innerchr4:133974883..134011840hg19UCSC Ensembl
Outerchr4:133974846..134011890hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3837045
hg1937045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675861
Supporting Variants
SamplesHG00335
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5866075
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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