A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929633



Internal ID21349702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26590410..26590410hg38UCSC Ensembl
chr8:26447926..26447926hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204398
SamplesHG002
Known GenesDPYSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929633
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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