A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274130



Internal ID20483348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127330992..127331289hg38UCSC Ensembl
chr8:128343237..128343534hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274130
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