A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258057



Internal ID21400288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62423471..62486004hg38UCSC Ensembl
chr9:46734772..46797305hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3862534
hg1962534
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730187
Supporting Variants
SamplesNA19239
Known GenesKGFLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258057
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