A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570498



Internal ID21762541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28089448..28089513hg38UCSC Ensembl
chr6:28057226..28057291hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012788
Supporting Variants
Samples
Known GenesZNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570498
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