A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046087



Internal ID20613127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28251830..28386685hg38UCSC Ensembl
chr19:28742737..28877592hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38134856
hg19134856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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