A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058676



Internal ID20625716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22248385..22257267hg38UCSC Ensembl
chr1:22574878..22583760hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg388883
hg198883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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