A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034978



Internal ID21944321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66474604..66474693hg38UCSC Ensembl
chr16:66508507..66508596hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627261
Samples
Known GenesBEAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034978
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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