A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289596



Internal ID20498814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128452915..128459028hg38UCSC Ensembl
chr8:129465161..129471274hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289596
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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