A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753034



Internal ID20528894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167600082..167600082hg38UCSC Ensembl
chr5:167027087..167027087hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278443
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753034
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