A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743679



Internal ID20519668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39357619..39357682hg38UCSC Ensembl
chr22:39753624..39753687hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289917
Samples
Known GenesSYNGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743679
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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