A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005589



Internal ID21914932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73011233..73012419hg38UCSC Ensembl
chr9:75626149..75627335hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005589
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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