A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973769



Internal ID22748704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69861554..69861554hg38UCSC Ensembl
chr18:67528790..67528790hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973769
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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