A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044474



Internal ID20611514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16257123..16257694hg38UCSC Ensembl
chr19:16367934..16368505hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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