A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951796



Internal ID21371865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44926026..44926026hg38UCSC Ensembl
chr22:45321906..45321906hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187450
SamplesHG002
Known GenesPHF21B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951796
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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