A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105447



Internal ID21512803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:472045..573542hg38UCSC Ensembl
chr19:472045..573542hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38101498
hg19101498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668357
Supporting Variants
Samples
Known GenesBSG, CDC34, GZMM, MADCAM1, ODF3L2, TPGS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105447
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer