A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968191



Internal ID22743126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35638908..35638908hg38UCSC Ensembl
chr19:36129810..36129810hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968191
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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