A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256077



Internal ID21398520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187414589..187424879hg38UCSC Ensembl
chr3:187132377..187142667hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3810291
hg1910291
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256077
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