A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950925



Internal ID21370994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3889350..3889350hg38UCSC Ensembl
chr16:3939351..3939351hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193878
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950925
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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