A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267344



Internal ID20476562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60005142..60016688hg38UCSC Ensembl
chr18:57672374..57683920hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3811547
hg1911547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267344
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