A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048223



Internal ID21957456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5609367..5609486hg38UCSC Ensembl
chr19:5609378..5609497hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627644
Samples
Known GenesSAFB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048223
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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