A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628950



Internal ID21820997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16104090..16104216hg38UCSC Ensembl
chr19:16214900..16215026hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628950
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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