A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088560



Internal ID21997793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13605521..13605521hg38UCSC Ensembl
chr9:13605520..13605520hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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