A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293283



Internal ID20502501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191584..170191850hg38UCSC Ensembl
chr6:170506808..170507074hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293283
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