A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765705



Internal ID20541565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84032730..84032730hg38UCSC Ensembl
chr1:84498413..84498413hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765705
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