A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257056



Internal ID21398785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179637491..179655580hg38UCSC Ensembl
chr5:179064492..179082581hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3818090
hg1918090
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730180
Supporting Variants
SamplesHG00514
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257056
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