A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067492



Internal ID21976725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99879868..99879868hg38UCSC Ensembl
chr4:100801025..100801025hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547765
Samples
Known GenesLAMTOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067492
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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