A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037979



Internal ID21947322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29577425..29585138hg38UCSC Ensembl
chr16:29588746..29596459hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387714
hg197714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037979
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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