A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052006



Internal ID21961239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6489811..6490926hg38UCSC Ensembl
chr19:6489822..6490937hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052006
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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