A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951274



Internal ID21371343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126260422..126260422hg38UCSC Ensembl
chr3:125979265..125979265hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189868
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951274
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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