A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272829



Internal ID20482047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24029424..24029595hg38UCSC Ensembl
chr6:24029652..24029823hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272829
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