A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105570



Internal ID22014803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743211..43743211hg38UCSC Ensembl
chr21:45163092..45163092hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640031
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105570
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