A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081319



Internal ID21490293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60516161..60516161hg38UCSC Ensembl
chr15:60808360..60808360hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653358
Supporting Variants
SamplesNA19238
Known GenesRORA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081319
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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