A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5799532



Internal ID8776935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107127990..107129150hg38UCSC Ensembl
Outerchr3:107127807..107129334hg38UCSC Ensembl
Innerchr3:106846837..106847997hg19UCSC Ensembl
Outerchr3:106846654..106848181hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg381528
hg191528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665865
Supporting Variants
SamplesHG00512
Known GenesLINC00882
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5799532
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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