A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873236



Internal ID22648181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:415088..425349hg38UCSC Ensembl
chr17:264879..275140hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810262
hg1910262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473783, nssv17478240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873236
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