A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742890



Internal ID20518875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365903..56366000hg38UCSC Ensembl
chr20:54940959..54941056hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274734
Samples
Known GenesFAM210B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742890
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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