A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124814



Internal ID20691854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121318485..121366345hg38UCSC Ensembl
chr5:120654180..120702040hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3847861
hg1947861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414818
Supporting Variants
Samples
Known GenesLOC102467226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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