A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049198



Internal ID20616238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55537736..55547137hg38UCSC Ensembl
chr19:56049103..56058503hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg389402
hg199401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532089
Supporting Variants
Samples
Known GenesSBK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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