A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101582



Internal ID21401441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62808281..62808281hg38UCSC Ensembl
chr18:60475514..60475514hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655101
Supporting Variants
SamplesHG00096
Known GenesPHLPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101582
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