A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044111



Internal ID21953402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16540632..16540957hg38UCSC Ensembl
chr19:16651443..16651768hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630777
Samples
Known GenesCHERP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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