A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287151



Internal ID20496369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66803440..66803440hg38UCSC Ensembl
chr8:67715675..67715675hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764554
Supporting Variants
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287151
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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