A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102633



Internal ID22011866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30402758..30402758hg38UCSC Ensembl
chr22:30798747..30798747hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648992
Samples
Known GenesSEC14L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102633
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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