A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587796



Internal ID21779839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125557649..125557649hg38UCSC Ensembl
chr9:128319928..128319928hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083284
Supporting Variants
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587796
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