A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044674



Internal ID20611714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72550690..72551263hg38UCSC Ensembl
chr18:70217925..70218498hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00176


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