A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11160813



Internal ID4433679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139207934..139226853hg38UCSC Ensembl
chr3:138926776..138945695hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3818920
hg1918920
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597934
Supporting Variants
SamplesHG03945
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11160813
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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