A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11179821



Internal ID1181637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149123365..149138174hg38UCSC Ensembl
Innerchr3:149123365..149138174hg38UCSC Ensembl
Outerchr3:149123326..149138242hg38UCSC Ensembl
chr3:148841152..148855961hg19UCSC Ensembl
Innerchr3:148841152..148855961hg19UCSC Ensembl
Outerchr3:148841113..148856029hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3814810
hg1914810
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598139
Supporting Variants
SamplesNA20799
Known GenesHPS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11179821
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