A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012901



Internal ID21922244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16502436..16719316hg38UCSC Ensembl
chr8:16359945..16576825hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38216881
hg19216881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012901
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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