A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739684



Internal ID20515659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591767..31592045hg38UCSC Ensembl
chr22:31987753..31988031hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268333
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739684
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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