A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268166



Internal ID20477384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70063231..70063350hg38UCSC Ensembl
chr8:70975466..70975585hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737417
Supporting Variants
Samples
Known GenesPRDM14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268166
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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