A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191752



Internal ID21330615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125824766..125824766hg38UCSC Ensembl
chr10:127513335..127513335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936645
Supporting Variants
SamplesHG002
Known GenesBCCIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191752
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