A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005647



Internal ID21914990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32478258..32478337hg38UCSC Ensembl
chr9:32478256..32478335hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584710
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005647
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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