A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267054



Internal ID20476272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87689405..87689405hg38UCSC Ensembl
chr10:89449162..89449162hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767316
Supporting Variants
Samples
Known GenesPAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267054
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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