A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089703



Internal ID21998936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122324307..122324307hg38UCSC Ensembl
chr9:125086586..125086586hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382688
hg192688
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089703
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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