A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267852



Internal ID20477070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100753039..100753102hg38UCSC Ensembl
chr8:101765267..101765330hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267852
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