A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103765



Internal ID22012998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20731512..20731512hg38UCSC Ensembl
chr22:21085800..21085800hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645080
Samples
Known GenesPI4KA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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