A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975789



Internal ID22750724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74178512..74178512hg38UCSC Ensembl
chr18:71845747..71845747hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975789
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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