A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625460



Internal ID7012294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16894335..16905752hg38UCSC Ensembl
Innerchr11:16894335..16905752hg38UCSC Ensembl
Outerchr11:16893835..16906252hg38UCSC Ensembl
chr11:16915882..16927299hg19UCSC Ensembl
Innerchr11:16915882..16927299hg19UCSC Ensembl
Outerchr11:16915382..16927799hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811418
hg1911418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14037357, essv14037356, essv14037355, essv14037354
SamplesNA19057, NA19068, NA18956, NA19011
Known GenesPLEKHA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625460
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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