A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090367



Internal ID21469719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60700569..60700569hg38UCSC Ensembl
chr15:60992768..60992768hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648706
Supporting Variants
SamplesHG03125
Known GenesRORA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090367
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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