A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097170



Internal ID22006403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100808079..100808079hg38UCSC Ensembl
chr9:103570361..103570361hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097170
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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