A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759107



Internal ID20534967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25603923..25603923hg38UCSC Ensembl
chr1:25930414..25930414hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759107
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