A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941643



Internal ID21361713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41306199..41306199hg38UCSC Ensembl
chr3:41347690..41347690hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189717
SamplesHG002
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941643
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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