A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633007



Internal ID7019817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86323265..86324410hg38UCSC Ensembl
Innerchr13:86323265..86324410hg38UCSC Ensembl
Outerchr13:86322955..86324628hg38UCSC Ensembl
chr13:86975520..86976665hg19UCSC Ensembl
Innerchr13:86975520..86976665hg19UCSC Ensembl
Outerchr13:86975210..86976883hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14829165, essv14829173, essv14829162, essv14829172, essv14829166, essv14829157, essv14829155, essv14829160, essv14829167, essv14829170, essv14829156, essv14829163, essv14829154, essv14829168, essv14829153, essv14829174, essv14829171, essv14829152, essv14829169, essv14829164, essv14829158, essv14829159, essv14829161
SamplesHG03690, HG03812, HG03616, HG03836, HG04206, NA20911, HG03234, HG04070, HG03594, HG03868, HG03746, HG04238, HG03814, HG03861, HG03007, HG03730, NA21117, HG04099, HG03973, HG03642, HG03716, HG03684, NA20772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633007
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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