A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257465



Internal ID21398021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50117497..50343753hg38UCSC Ensembl
chr11:50076668..50302924hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38226257
hg19226257
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730168
Supporting Variants
SamplesHG00512
Known GenesLOC441601
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257465
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