A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150195



Internal ID21503226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33684430..33694208hg38UCSC Ensembl
chr6:33652207..33661985hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389779
hg199779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671337
Supporting Variants
SamplesNA19239
Known GenesITPR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150195
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