A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356258



Internal ID22581927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132891911..133122202hg38UCSC Ensembl
chr10:134705415..134935706hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38230292
hg19230292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926627
Supporting Variants
Samples
Known GenesGPR123, LOC399829, TTC40
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356258
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.50


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