A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989997



Internal ID60742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151015955..151016885hg38UCSC Ensembl
chr6:151337091..151338021hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557493
Supporting Variants
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989997
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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