A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453954



Internal ID22511829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95905199..95908543hg38UCSC Ensembl
chr13:96557453..96560797hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383345
hg193345
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849731
Supporting Variants
Samples
Known GenesUGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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