A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098020



Internal ID22007253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4540935..4540935hg38UCSC Ensembl
chr17:4444230..4444230hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624440
Samples
Known GenesMYBBP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098020
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