A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745329



Internal ID20521336
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 StatusM
Merged Variants
Supporting Variantsnssv16267808
Samples
Known GenesACOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745329
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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