A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258489



Internal ID21399494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187418526..187426206hg38UCSC Ensembl
chr3:187136314..187143994hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg387681
hg197681
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258489
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