A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018616



Internal ID21927959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121954013..121955604hg38UCSC Ensembl
chr8:122966252..122967843hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381592
hg191592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018616
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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