A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037367



Internal ID21946710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4149357..4160177hg38UCSC Ensembl
chr16:4199358..4210178hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810821
hg1910821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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