A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930882



Internal ID21350952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43911562..43911562hg38UCSC Ensembl
chr1:44377234..44377234hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193395
SamplesHG002
Known GenesST3GAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930882
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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