A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749873



Internal ID20525908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166739875..166739961hg38UCSC Ensembl
chr1:166709112..166709198hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749873
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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