A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935041



Internal ID21355111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87145110..87145110hg38UCSC Ensembl
chr16:87178716..87178716hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184267
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935041
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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