A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751029



Internal ID20526889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89968677..89968677hg38UCSC Ensembl
chr1:90434236..90434236hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751029
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