A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239746



Internal ID20806786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79857017..79857956hg38UCSC Ensembl
chr15:80149359..80150298hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591397
Supporting Variants
Samples
Known GenesMTHFS, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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