A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289917



Internal ID20499135
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 StatusS
Merged Variantsnsv4743679
Supporting Variants
Samples
Known GenesSYNGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289917
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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