A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043171



Internal ID21952482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10182391..10182444hg38UCSC Ensembl
chr19:10293067..10293120hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632492
Samples
Known GenesDNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043171
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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