A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091129



Internal ID22000362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35578881..35578881hg38UCSC Ensembl
chr9:35578878..35578878hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091129
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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