A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077332



Internal ID21986565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99879799..99879799hg38UCSC Ensembl
chr4:100800956..100800956hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547335
Samples
Known GenesLAMTOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077332
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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