A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760767



Internal ID20536627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36706207..36706207hg38UCSC Ensembl
chr22:37102252..37102252hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760767
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer