A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843753



Internal ID22618688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131323402..131330049hg38UCSC Ensembl
chr6:131644542..131651189hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386648
hg196648
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1800n209
Supporting Variantsnssv17501588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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