A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046130



Internal ID21955375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10593108..10593868hg38UCSC Ensembl
chr19:10703784..10704544hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046130
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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