A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041374



Internal ID21950709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15334846..15335184hg38UCSC Ensembl
chr19:15445657..15445995hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041374
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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