A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875391



Internal ID22650348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77925442..77927593hg38UCSC Ensembl
chr17:75921524..75923675hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875391
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