A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902815



Internal ID2690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54933180..54934712hg38UCSC Ensembl
chr1:55398853..55400385hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902815
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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