A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049550



Internal ID20616590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9829501..9832100hg38UCSC Ensembl
chr19:9940177..9942776hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522910
Supporting Variants
Samples
Known GenesUBL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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