A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070226



Internal ID21979459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99879940..99879940hg38UCSC Ensembl
chr4:100801097..100801097hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548370
Samples
Known GenesLAMTOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070226
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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