A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058391



Internal ID20625431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225950718..225952793hg38UCSC Ensembl
chr1:226138418..226140493hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg382076
hg192076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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