A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101893



Internal ID22011126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38110042..38110042hg38UCSC Ensembl
chr22:38506049..38506049hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381879
hg191879
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640902
Samples
Known GenesBAIAP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101893
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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