A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982019



Internal ID21891362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19642982..19643130hg38UCSC Ensembl
chr1:19969476..19969624hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519390
Samples
Known GenesMINOS1-NBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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