A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1091e214



Internal ID22756985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35351678..35366840hg38UCSC Ensembl
chr5:35351780..35366942hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3815163
hg1915163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3604700, esv3604699
SamplesNA20882, NA20900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1091e214
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