A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089885



Internal ID21999118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74690695..74690695hg38UCSC Ensembl
chr9:77305611..77305611hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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