A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890756



Internal ID22665785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113819236..113820355hg38UCSC Ensembl
chr6:114140439..114141558hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890756
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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