A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134942



Internal ID21497743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195620740..195980207hg38UCSC Ensembl
chr3:195347611..195707078hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38359468
hg19359468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667176
Supporting Variants
SamplesNA19238
Known GenesMIR570, MIR6829, MUC20, MUC4, SDHAP1, SDHAP2, TNK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134942
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