A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746876



Internal ID20522892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22273625..22273761hg38UCSC Ensembl
chr18:19853588..19853724hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746876
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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