A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14278460



Internal ID2621690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108931729..108933404hg38UCSC Ensembl
Innerchr11:108931729..108933404hg38UCSC Ensembl
Outerchr11:108931473..108933660hg38UCSC Ensembl
chr11:108802456..108804131hg19UCSC Ensembl
Innerchr11:108802456..108804131hg19UCSC Ensembl
Outerchr11:108802200..108804387hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627690
Supporting Variants
SamplesHG02318
Known GenesDDX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14278460
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