A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042090



Internal ID20609130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48775301..48786000hg38UCSC Ensembl
chr18:46301672..46312371hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518273
Supporting Variants
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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