A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058541



Internal ID21967774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30534471..30534558hg38UCSC Ensembl
chr22:30930458..30930545hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643847
Samples
Known GenesSEC14L6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058541
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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