A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459353



Internal ID21116906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57881057..57890493hg38UCSC Ensembl
chr11:57648529..57657965hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg389437
hg199437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459353
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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