A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108426



Internal ID22017660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5996275..5996275hg38UCSC Ensembl
chr19:5996286..5996286hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623469
Samples
Known GenesLOC100128568, RFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108426
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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