A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026838



Internal ID20593878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79905143..79906565hg38UCSC Ensembl
chr15:80197485..80198907hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381423
hg191423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497979
Supporting Variants
Samples
Known GenesST20, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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