A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026837



Internal ID20593877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79873801..79879100hg38UCSC Ensembl
chr15:80166143..80171442hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500062
Supporting Variants
Samples
Known GenesMTHFS, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00372


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