A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626585



Internal ID7013417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61669044..61678449hg38UCSC Ensembl
Innerchr11:61669105..61678388hg38UCSC Ensembl
Outerchr11:61668983..61678510hg38UCSC Ensembl
chr11:61436516..61445921hg19UCSC Ensembl
Innerchr11:61436577..61445860hg19UCSC Ensembl
Outerchr11:61436455..61445982hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg389406
hg199406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14178520, essv14178521
SamplesNA19078, NA19011
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626585
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