A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007915



Internal ID21917258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42942055..43003989hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3861935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007915
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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