A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14029127



Internal ID5099365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11006296..11009209hg38UCSC Ensembl
Innerchr11:11006296..11009209hg38UCSC Ensembl
Outerchr11:11006097..11009419hg38UCSC Ensembl
chr11:11027843..11030756hg19UCSC Ensembl
Innerchr11:11027843..11030756hg19UCSC Ensembl
Outerchr11:11027644..11030966hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382914
hg192914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625369
Supporting Variants
SamplesNA18552
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14029127
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