A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086078



Internal ID21995311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90550383..90550383hg38UCSC Ensembl
chr9:93312665..93312665hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577849
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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