A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551509



Internal ID324956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35729996..35730000hg38UCSC Ensembl
chr9:35729993..35729997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023669
Samples
Known GenesTLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551509
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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