A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875375



Internal ID22650332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44087707..44089906hg38UCSC Ensembl
chr21:45507588..45509787hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488925, nssv17488924
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875375
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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