A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043661



Internal ID21952955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3513180..3513251hg38UCSC Ensembl
chr19:3513178..3513249hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623862
Samples
Known GenesFZR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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