A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352396



Internal ID22578065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103354716..103423522hg38UCSC Ensembl
chr10:105114473..105183279hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3868807
hg1968807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909873
Supporting Variants
Samples
Known GenesMIR1307, PDCD11, TAF5, USMG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352396
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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