A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618646



Internal ID7005528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122259882..122315583hg38UCSC Ensembl
Innerchr8:122259882..122315583hg38UCSC Ensembl
Outerchr8:122259382..122316083hg38UCSC Ensembl
chr8:123272121..123327822hg19UCSC Ensembl
Innerchr8:123272121..123327822hg19UCSC Ensembl
Outerchr8:123271621..123328322hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3855702
hg1955702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13308843
SamplesHG04134
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618646
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