A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625474



Internal ID7012308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17299682..17306699hg38UCSC Ensembl
Innerchr11:17299682..17306699hg38UCSC Ensembl
Outerchr11:17299271..17307134hg38UCSC Ensembl
chr11:17321229..17328246hg19UCSC Ensembl
Innerchr11:17321229..17328246hg19UCSC Ensembl
Outerchr11:17320818..17328681hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387018
hg197018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14040152, essv14040153
SamplesHG01506, NA19072
Known GenesNUCB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625474
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