A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5898633



Internal ID8876036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152247276..152252135hg38UCSC Ensembl
Outerchr3:152247239..152252185hg38UCSC Ensembl
Innerchr3:151965065..151969924hg19UCSC Ensembl
Outerchr3:151965028..151969974hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384947
hg194947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662422
Supporting Variants
SamplesNA20819
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5898633
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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