A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044377



Internal ID21953660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151769293..151769293hg38UCSC Ensembl
chr1:151741769..151741769hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531917
Samples
Known GenesOAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044377
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer