A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926368



Internal ID21346438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233513863..233513863hg38UCSC Ensembl
chr1:233649609..233649609hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189424
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926368
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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