A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945108



Internal ID21365177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22585635..22585635hg38UCSC Ensembl
chr8:22443148..22443148hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204045
SamplesHG002
Known GenesPDLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945108
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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