A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604699



Internal ID6991727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35351678..35365443hg38UCSC Ensembl
Innerchr5:35352178..35364943hg38UCSC Ensembl
Outerchr5:35350678..35366443hg38UCSC Ensembl
chr5:35351780..35365545hg19UCSC Ensembl
Innerchr5:35352280..35365045hg19UCSC Ensembl
Outerchr5:35350780..35366545hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3813766
hg1913766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1091e214
Supporting Variantsessv11868489, essv11868490
SamplesNA20882, NA20900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604699
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