A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067173



Internal ID21976406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10437..10437hg38UCSC Ensembl
chr9:10437..10437hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067173
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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