A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627613



Internal ID7014441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105542383..105545842hg38UCSC Ensembl
Innerchr11:105542383..105545842hg38UCSC Ensembl
Outerchr11:105542312..105546018hg38UCSC Ensembl
chr11:105413110..105416569hg19UCSC Ensembl
Innerchr11:105413110..105416569hg19UCSC Ensembl
Outerchr11:105413039..105416745hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383460
hg193460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14268515, essv14268516, essv14268513, essv14268519, essv14268518, essv14268514, essv14268520, essv14268512, essv14268511, essv14268510, essv14268517
SamplesHG01985, NA18502, NA19222, NA19703, HG02583, HG03091, HG02645, HG03520, HG02642, HG03472, NA19206
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627613
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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