A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5541662



Internal ID8749110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99327993..99337159hg38UCSC Ensembl
Outerchr3:99327836..99337312hg38UCSC Ensembl
Innerchr3:99046837..99056003hg19UCSC Ensembl
Outerchr3:99046680..99056156hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg389477
hg199477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664040
Supporting Variants
SamplesHG00139
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5541662
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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