A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096187



Internal ID22005420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64046383..64046383hg38UCSC Ensembl
chr15:64338582..64338582hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096187
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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