A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091257



Internal ID22000490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111916..23111916hg38UCSC Ensembl
chr10:23400845..23400845hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578893
Samples
Known GenesMSRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091257
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