A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047508



Internal ID21956741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4843188..4845893hg38UCSC Ensembl
chr19:4843200..4845905hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382706
hg192706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621507
Samples
Known GenesPLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047508
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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