A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947493



Internal ID22722999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63512682..63523701hg38UCSC Ensembl
chr18:61179915..61190934hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3811020
hg1911020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947493
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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