A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604361



Internal ID21796408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60516016..60516016hg38UCSC Ensembl
chr15:60808215..60808215hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092077
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604361
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