A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058012



Internal ID20625052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216095101..216258300hg38UCSC Ensembl
chr1:216268443..216431642hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38163200
hg19163200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318677
Supporting Variants
Samples
Known GenesUSH2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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