A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055555



Internal ID21964788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55542990..55543246hg38UCSC Ensembl
chr19:56054356..56054612hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624658
Samples
Known GenesSBK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055555
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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