A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928042



Internal ID21348112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70239932..70239932hg38UCSC Ensembl
chr10:71999688..71999688hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190428
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928042
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer