A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058735



Internal ID20625775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232309683..232368271hg38UCSC Ensembl
chr1:232445429..232504017hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3858589
hg1958589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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