A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083007



Internal ID21992240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120835133..120835133hg38UCSC Ensembl
chr9:123597411..123597411hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596672
Samples
Known GenesPSMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083007
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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