A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970802



Internal ID47866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135813726..135825461hg38UCSC Ensembl
chr6:136134864..136146599hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3811736
hg1911736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970802
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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