A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096871



Internal ID21512678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34540657..34562467hg38UCSC Ensembl
chr14:35009863..35031673hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821811
hg1921811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664918
Supporting Variants
Samples
Known GenesSNX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096871
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