A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767316



Internal ID20543176
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 StatusM
Merged Variants
Supporting Variantsnssv16267054
Samples
Known GenesPAPSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767316
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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