A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11160814



Internal ID4340609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139208260..139226732hg38UCSC Ensembl
Innerchr3:139208760..139226232hg38UCSC Ensembl
Outerchr3:139207260..139227732hg38UCSC Ensembl
chr3:138927102..138945574hg19UCSC Ensembl
Innerchr3:138927602..138945074hg19UCSC Ensembl
Outerchr3:138926102..138946574hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3818473
hg1918473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597935
Supporting Variants
SamplesHG03882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11160814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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