A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865532



Internal ID13317908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122270886..122270899hg38UCSC Ensembl
Innerchr11:122270888..122270897hg38UCSC Ensembl
Outerchr11:122270884..122270901hg38UCSC Ensembl
chr11:122141594..122141607hg19UCSC Ensembl
Innerchr11:122141596..122141605hg19UCSC Ensembl
Outerchr11:122141592..122141609hg19UCSC Ensembl
chr11:121646804..121646817hg18UCSC Ensembl
Innerchr11:121646806..121646815hg18UCSC Ensembl
Outerchr11:121646802..121646819hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3366755
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865532
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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