A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912982



Internal ID9401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47718633..47720064hg38UCSC Ensembl
chr2:47945772..47947203hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912982
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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