A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560426



Internal ID21884781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73660475..73660527hg38UCSC Ensembl
chr6:74370198..74370250hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560426
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