A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007360



Internal ID21916703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110335475..110335586hg38UCSC Ensembl
chr6:110656678..110656789hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577426
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007360
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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