A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257073



Internal ID21398830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41794069..41872782hg38UCSC Ensembl
chr9:65683178..65761243hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3878714
hg1978066
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730078
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257073
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