A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099890



Internal ID22009123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134710951..134710951hg38UCSC Ensembl
chr9:137602797..137602797hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590538
Samples
Known GenesCOL5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099890
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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