A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472331



Internal ID22530223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79873382..79879092hg38UCSC Ensembl
chr15:80165724..80171434hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385711
hg195711
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854865
Supporting Variants
Samples
Known GenesMTHFS, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472331
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