A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027858



Internal ID21937201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20820505..20820654hg38UCSC Ensembl
chr16:20831827..20831976hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600866
Samples
Known GenesLOC81691
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027858
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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