A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273871



Internal ID20483089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31514269..31514384hg38UCSC Ensembl
chr22:31910255..31910370hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748644
Supporting Variants
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273871
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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