A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633405



Internal ID21825452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86554866..86558204hg38UCSC Ensembl
chr16:86588472..86591810hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383339
hg193339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039731
Supporting Variants
Samples
Known GenesFLJ30679, MTHFSD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633405
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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