A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625117



Internal ID7011955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1806902..1811707hg38UCSC Ensembl
Innerchr11:1807402..1811207hg38UCSC Ensembl
Outerchr11:1805902..1812707hg38UCSC Ensembl
chr11:1828132..1832937hg19UCSC Ensembl
Innerchr11:1828632..1832437hg19UCSC Ensembl
Outerchr11:1827132..1833937hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384806
hg194806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993512, essv13993511, essv13993510, essv13993507, essv13993509, essv13993508
SamplesNA18519, HG03027, HG03311, NA19436, NA19072, HG03063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625117
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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