A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11093486



Internal ID4307054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106163036..106179868hg38UCSC Ensembl
Innerchr3:106163044..106179860hg38UCSC Ensembl
Outerchr3:106163028..106179876hg38UCSC Ensembl
chr3:105881883..105898715hg19UCSC Ensembl
Innerchr3:105881891..105898707hg19UCSC Ensembl
Outerchr3:105881875..105898723hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3816833
hg1916833
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597282
Supporting Variants
SamplesHG03862
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11093486
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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