A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936730



Internal ID21356799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26278986..26278986hg38UCSC Ensembl
chr22:26674952..26674952hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188778
SamplesHG002
Known GenesSEZ6L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936730
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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