A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949608



Internal ID21369677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150221777..150221777hg38UCSC Ensembl
chr3:149939564..149939564hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189891
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949608
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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