A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878357



Internal ID22653322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33975807..34007934hg38UCSC Ensembl
chr18:31555771..31587898hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3832128
hg1932128
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477907
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878357
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