A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090730



Internal ID21999963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64371888..64371888hg38UCSC Ensembl
chr15:64664087..64664087hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598878
Samples
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090730
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