A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059175



Internal ID20626215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:242996401..243120600hg38UCSC Ensembl
chr1:243159703..243283902hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38124200
hg19124200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315725
Supporting Variants
Samples
Known GenesLOC731275
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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