A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573276



Internal ID21765319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28327781..28328343hg38UCSC Ensembl
chr8:28185298..28185860hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000966
Supporting Variants
Samples
Known GenesPNOC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573276
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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