A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751886



Internal ID20527746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209990536..209990536hg38UCSC Ensembl
chr1:210163881..210163881hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281710
Samples
Known GenesSYT14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751886
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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