A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018048



Internal ID21927391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80484657..80486263hg38UCSC Ensembl
chr9:83099572..83101178hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381607
hg191607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018048
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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