A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258122



Internal ID21399810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146228162..149314918hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383086757
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730271
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258122
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer