A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535193



Internal ID310884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99879157..99879194hg38UCSC Ensembl
chr4:100800314..100800351hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953255
Samples
Known GenesLAMTOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535193
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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