A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841678



Internal ID22616613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136207196..136210395hg38UCSC Ensembl
chr5:135542884..135546083hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841678
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