A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854496



Internal ID22629431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36408725..36411643hg38UCSC Ensembl
chr8:36266243..36269161hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382919
hg192919
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2006n209
Supporting Variantsnssv17509179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854496
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