A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097954



Internal ID22007187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119158992..119158992hg38UCSC Ensembl
chr10:120918504..120918504hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584345
Samples
Known GenesSFXN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097954
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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