A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941214



Internal ID28185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151926634..151987639hg38UCSC Ensembl
chr3:151644422..151705428hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3861006
hg1961007
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941214
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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