A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058838



Internal ID20625878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235079026..235088788hg38UCSC Ensembl
chr1:235242340..235252103hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg389763
hg199764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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