A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059208



Internal ID20626248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228421085..228445457hg38UCSC Ensembl
chr1:228608786..228633158hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3824373
hg1924373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326405
Supporting Variants
Samples
Known GenesHIST3H3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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