A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091286



Internal ID22000519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10792059..10792059hg38UCSC Ensembl
chr10:10834022..10834022hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589758
Samples
Known GenesSFTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091286
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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