A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052878



Internal ID21962111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17437719..17439195hg38UCSC Ensembl
chr19:17548528..17550004hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381477
hg191477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624090
Samples
Known GenesTMEM221
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052878
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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