A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367167



Internal ID22592836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131049156..131126884hg38UCSC Ensembl
chr10:132847419..132925147hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3877729
hg1977729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915688
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367167
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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