A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579391



Internal ID21771434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125458890..125458890hg38UCSC Ensembl
chr9:128221169..128221169hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097327
Supporting Variants
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579391
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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