A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580137



Internal ID21772180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126624745..126624745hg38UCSC Ensembl
chr9:129387024..129387024hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085684
Supporting Variants
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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