A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888377



Internal ID22663382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145515873..145586966hg38UCSC Ensembl
chr6:145837009..145908102hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3871094
hg1971094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888377
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