A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839237



Internal ID22614172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26045249..26054171hg38UCSC Ensembl
chr4:26046871..26055793hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388923
hg198923
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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