A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456622



Internal ID21114175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59367217..59367922hg38UCSC Ensembl
chr11:59134690..59135395hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456622
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