A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935745



Internal ID21355815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35343305..35343305hg38UCSC Ensembl
chr22:35739298..35739298hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187402
SamplesHG002
Known GenesTOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935745
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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