A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568180



Internal ID21760223
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 StatusS
Merged Variantsnsv6018809
Supporting Variants
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568180
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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