A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841359



Internal ID22616294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120578690..120579789hg38UCSC Ensembl
chr5:119914385..119915484hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493793, nssv17493794
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841359
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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