A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256313



Internal ID21400765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43231581..43322790hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3891210
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730111
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256313
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