A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11098103



Internal ID4035394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109393274..109396239hg38UCSC Ensembl
Innerchr3:109393424..109396089hg38UCSC Ensembl
Outerchr3:109393124..109396389hg38UCSC Ensembl
chr3:109112121..109115086hg19UCSC Ensembl
Innerchr3:109112271..109114936hg19UCSC Ensembl
Outerchr3:109111971..109115236hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597348
Supporting Variants
SamplesHG03686
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11098103
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer