A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874853



Internal ID22649807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95584316..95590100hg38UCSC Ensembl
chr15:96127545..96133329hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385785
hg195785
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874853
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