A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408885



Internal ID22466755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54959207..54960663hg38UCSC Ensembl
chr19:55470575..55472031hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930346
Supporting Variants
Samples
Known GenesRNU6-35P, RNU6-64P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408885
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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