A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757225



Internal ID20533085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1934249..1934249hg38UCSC Ensembl
chr1:1865688..1865688hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757225
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