A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016363



Internal ID21925706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93046588..93046707hg38UCSC Ensembl
chr9:95808870..95808989hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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