A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14220599



Internal ID1974687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84761611..84798317hg38UCSC Ensembl
Innerchr11:84761626..84798303hg38UCSC Ensembl
Outerchr11:84761597..84798332hg38UCSC Ensembl
chr11:84472654..84509360hg19UCSC Ensembl
Innerchr11:84472669..84509346hg19UCSC Ensembl
Outerchr11:84472640..84509375hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3836707
hg1936707
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627050
Supporting Variants
SamplesHG01841
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14220599
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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