A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039731



Internal ID21949074
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 StatusM
Merged Variants
Supporting Variantsnssv17633405
Samples
Known GenesFLJ30679, MTHFSD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039731
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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