A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761771



Internal ID20537631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150506570..150506570hg38UCSC Ensembl
chr1:150479046..150479046hg19UCSC 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 Variantsnssv16287360
Samples
Known GenesTARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761771
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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