A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110133



Internal ID22019366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39517063..39517063hg38UCSC Ensembl
chr19:40007703..40007703hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382570
hg192570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637349
Samples
Known GenesSELV
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110133
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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