A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003930



Internal ID21913273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91381555..91384300hg38UCSC Ensembl
chr9:94143837..94146582hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382746
hg192746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003930
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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