A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267808



Internal ID20477026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45847564..45847672hg38UCSC Ensembl
chr20:44476203..44476311hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745329
Supporting Variants
Samples
Known GenesACOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267808
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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