A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633463



Internal ID7020272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106305276..106336738hg38UCSC Ensembl
Innerchr13:106305310..106336705hg38UCSC Ensembl
Outerchr13:106305243..106336772hg38UCSC Ensembl
chr13:106957625..106989086hg19UCSC Ensembl
Innerchr13:106957659..106989053hg19UCSC Ensembl
Outerchr13:106957592..106989120hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3831463
hg1931462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv368e214
Supporting Variantsessv14890290
SamplesHG03118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633463
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