A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735196



Internal ID20511137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32000064..32000140hg38UCSC Ensembl
chr22:32396051..32396127hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735196
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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