A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838911



Internal ID22613846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24089369..24095274hg38UCSC Ensembl
chr4:24090992..24096897hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385906
hg195906
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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