A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627072



Internal ID7013902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85718727..85761134hg38UCSC Ensembl
Innerchr11:85718744..85761118hg38UCSC Ensembl
Outerchr11:85718711..85761151hg38UCSC Ensembl
chr11:85429770..85472177hg19UCSC Ensembl
Innerchr11:85429787..85472161hg19UCSC Ensembl
Outerchr11:85429754..85472194hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3842408
hg1942408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14221562
SamplesNA12761
Known GenesSYTL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627072
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