A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402027



Internal ID181400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131017052..131017103hg38UCSC Ensembl
chr9:133892439..133892490hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028924
Samples
Known GenesLAMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402027
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer