A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467878



Internal ID22525768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110834..131114363hg38UCSC Ensembl
chr10:132909097..132912626hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383530
hg193530
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850396
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467878
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