A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097513



Internal ID22006746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127862357..127862357hg38UCSC Ensembl
chr9:130624636..130624636hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097513
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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