A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032427



Internal ID21941770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67938424..67938808hg38UCSC Ensembl
chr16:67972327..67972711hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032427
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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