A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068355



Internal ID21977588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084343..150084343hg38UCSC Ensembl
chr5:149463906..149463906hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575483
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068355
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