A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839324



Internal ID22614259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45469536..45495199hg38UCSC Ensembl
chr4:45471553..45497216hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3825664
hg1925664
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495175, nssv17495176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839324
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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