A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040860



Internal ID20607900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2884312..2885544hg38UCSC Ensembl
chr18:2884310..2885542hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533797
Supporting Variants
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00091


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