A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622531



Internal ID21814578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40450452..40450522hg38UCSC Ensembl
chr19:40956359..40956429hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059793
Supporting Variants
Samples
Known GenesBLVRB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622531
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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