A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044695



Internal ID20611735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72746001..72747400hg38UCSC Ensembl
chr18:70413236..70414635hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534614
Supporting Variants
Samples
Known GenesNETO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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