A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055529



Internal ID21964762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3571139..3571214hg38UCSC Ensembl
chr19:3571137..3571212hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055529
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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