A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943449



Internal ID22718898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66998657..67041777hg38UCSC Ensembl
chr18:64665894..64709014hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3843121
hg1943121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943449
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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