A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239747



Internal ID20806787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79876388..79880080hg38UCSC Ensembl
chr15:80168730..80172422hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383693
hg193693
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578819
Supporting Variants
Samples
Known GenesMTHFS, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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