A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586573



Internal ID6974091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79239677..79246217hg38UCSC Ensembl
Innerchr1:79239727..79246167hg38UCSC Ensembl
Outerchr1:79239627..79246267hg38UCSC Ensembl
chr1:79705362..79711902hg19UCSC Ensembl
Innerchr1:79705412..79711852hg19UCSC Ensembl
Outerchr1:79705312..79711952hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg386541
hg196541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9986499, essv9986500
SamplesHG01586, HG01933
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586573
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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