A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050914



Internal ID20617954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111601923..111605230hg38UCSC Ensembl
chr1:112144545..112147852hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg383308
hg193308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319624
Supporting Variants
Samples
Known GenesLOC100129269
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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