A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256406



Internal ID21400799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146495389..146528423hg38UCSC Ensembl
chr1_gl000192_random:426576..459618hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3833035
hg1933043
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730271
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256406
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