A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257726



Internal ID21400001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195750062..195996876hg38UCSC Ensembl
chr3:195476933..195723747hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38246815
hg19246815
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730152
Supporting Variants
SamplesNA19238
Known GenesMIR6829, MUC4, SDHAP1, TNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257726
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