A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081495



Internal ID21990728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107809360..107809360hg38UCSC Ensembl
chr9:110571641..110571641hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081495
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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