A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983136



Internal ID56135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41198301..41249460hg38UCSC Ensembl
chr6:41166039..41217198hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3851160
hg1951160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147085
Supporting Variants
Samples
Known GenesTREML2, TREML3P, TREML4, TREML5P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983136
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.013429


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