A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043456



Internal ID21952760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10182425..10182499hg38UCSC Ensembl
chr19:10293101..10293175hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634283
Samples
Known GenesDNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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