A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626654



Internal ID6666804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63854693..63855199hg38UCSC Ensembl
Innerchr11:63854694..63855198hg38UCSC Ensembl
Outerchr11:63854692..63855200hg38UCSC Ensembl
chr11:63622165..63622671hg19UCSC Ensembl
Innerchr11:63622166..63622670hg19UCSC Ensembl
Outerchr11:63622164..63622672hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14184892, essv14184898, essv14184903, essv14184904, essv14184894, essv14184896, essv14184897, essv14184895, essv14184902, essv14184893, essv14184901, essv14184900, essv14184899
SamplesNA18602, NA18563, HG03874, HG02057, NA18956, NA19081, NA19084, NA18532, NA18943, HG01804, HG01846, HG02186, NA18957
Known GenesMARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626654
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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