A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022460



Internal ID21931803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3240730..3255470hg38UCSC Ensembl
chr16:3290730..3305470hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814741
hg1914741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598187
Samples
Known GenesMEFV
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022460
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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