A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905951



Internal ID22681144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137252647..137255769hg38UCSC Ensembl
chr6:137573784..137576906hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905951
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