A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626636



Internal ID21818683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67579274..67590686hg38UCSC Ensembl
chr16:67613177..67624589hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3811413
hg1911413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031796
Supporting Variants
Samples
Known GenesCTCF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626636
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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