A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045046



Internal ID20612086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17884348..17885037hg38UCSC Ensembl
chr19:17995157..17995846hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530834
Supporting Variants
Samples
Known GenesSLC5A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007


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