A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026977



Internal ID21936320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20414384..20493494hg38UCSC Ensembl
chr16:20425706..20504816hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3879111
hg1979111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617068
Samples
Known GenesACSM2A, ACSM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026977
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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