A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117670



Internal ID20684710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4544001..4552800hg38UCSC Ensembl
chr4:4545728..4554527hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357486
Supporting Variants
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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