A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995880



Internal ID21905223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1828280..1829303hg38UCSC Ensembl
chr4:1830007..1831030hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381024
hg191024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542997
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995880
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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