A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582153



Internal ID21774196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131032628..131032628hg38UCSC Ensembl
chr9:133908015..133908015hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097099
Supporting Variants
Samples
Known GenesLAMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582153
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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