A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027255



Internal ID21936598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54666388..54666633hg38UCSC Ensembl
chr16:54700300..54700545hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027255
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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