A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257438



Internal ID21398247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61785368..62149739hg38UCSC Ensembl
chr9:44958294..45250204hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38364372
hg19291911
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730187
Supporting Variants
SamplesHG00513
Known GenesFAM27C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257438
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