A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046086



Internal ID20613126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2824241..2832320hg38UCSC Ensembl
chr19:2824239..2832318hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388080
hg198080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519901
Supporting Variants
Samples
Known GenesZNF554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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