A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915397



Internal ID11004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100201783..100202355hg38UCSC Ensembl
chr2:100818245..100818817hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915397
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00921


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