A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612780



Internal ID21804827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66469692..66469692hg38UCSC Ensembl
chr15:66762030..66762030hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095797
Supporting Variants
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612780
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