A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937197



Internal ID22712560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72400188..72400357hg38UCSC Ensembl
chr18:70067423..70067592hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937197
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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