A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257621



Internal ID21399816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40691369..40868523hg38UCSC Ensembl
chr9:66664196..66821551hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38177155
hg19157356
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257621
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