A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647484



Internal ID21595789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14057591..14057591hg38UCSC Ensembl
chr19:14168403..14168403hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103143
SamplesHG02587
Known GenesPALM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647484
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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