A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018809



Internal ID21928152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151043978..151046802hg38UCSC Ensembl
chr6:151365114..151367938hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382825
hg192825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568180
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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