A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850396



Internal ID22625331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110834..131114363hg38UCSC Ensembl
chr10:132909097..132912626hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383530
hg193530
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467878, nssv17468523
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850396
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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